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Enterprse Desktop Mgmnt SpclstJob ID: 13223Location: El Paso, TXFull/Part Time: Full TimeRegular/Temporary: RegularAbout UTEPUTEP is a comprehensive public research university that is increasing access to excellent higher education. We advance discovery of public value and positively impact the health, culture, education, and economy of the community we serve.The University of Texas at El Paso is America's leading Hispanic-serving university. Located at the westernmost tip of Texas, where three states and two countries converge along the Rio Grande, 84% of our 24,000 students are Hispanic, and more than half are the first in their families to go to college. UTEP offers 172 bachelor's, master's and doctoral degree programs at the only open-access, top-tier research university in America.Position InformationHiring Department: VPIRPosting End Date: Open until filled. This posting may close once a sufficient number of qualified applications have been received.Hours: 40 hours per week, standard Monday- Friday 8:00am- 5:00pm, flexibility is required on evenings and weekendsFLSA status: ExemptEarliest Start Date: As soon as possible.Salary: $48,500 annuallyRequired Application Materials:• Resume• Cover LetterThe primary accountabilities are intended to describe the general content of and requirements of this position and are not intended to be an exhaustive statement of duties. Incumbents may perform all or some of the primary accountabilities listed. Specific tasks or responsibilities will be documented in the incumbents' performance objectives as outlined by the incumbents' immediate supervisor or manager. This position is security-sensitive and subject to Texas Education Code §51.215, which authorizes the employer to obtain criminal history record information. A valid driver's license issued by the State where the applicant resides and insurability as defined in UTS 157 may be required to perform the position's essential functions.Purpose of PositionProvides campus-wide desktop management support in an area of specialization.Essential FunctionsWorks directly with all areas of Information Technology department and computer lab managers to establish guidelines and policies for management of desktop computers.Creates group polices for computer management in Active Directory and other mobile device management (MDM) consoles.Establishes Group Policy Object (GPO) guidelines for the domain computers which includes GPOs created and applied at delegated Organization Units (OUs).Stays abreast of evolving technology in assigned area(s) to provide technical support to customers.Creates, implements, and maintains systems and reporting that enables the accurate inventory of hardware and software on UTEP owned computers.Supports and maintains Software License Manager servers for a variety of campus-wide licensed software.Provides reports and statistics on computers and their configurations.Researches, pilots, and implements new technologies to improve management of computers and mobile devices such as tablets.Assists the Office of Information Security with the distribution of patches and updates to PCs.Documents processes and procedures related to handling and support of UTEP computers.Assists Customer Support with desktop migration and computer imaging processes.Assists in providing lab managers and other related positions with OUs and delegation of security for distributed management of computers.Design and implements software deployment to computers in the Miners domain.Assists with special projects, new technologies, and deadlines.Complies with all State and University policies.Other duties as assigned. Supervisory Responsibilities:No supervisory responsibilities.QualificationsTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.Required Qualifications:Education: Associates degreeandExperience: Three (3) or more years of related experience and training working with personal computer maintenance or desktop management; experience with Microsoft Active Directory, management of group policies and other mobile device management consoles (MDM); or equivalent combination of education and experience.Preferred Qualifications: MCSE or MCSA certification.Additional InformationThe physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.While performing the duties of this job, the employee must frequently stand and walk. The employee must regularly sit; use hands to feel; reach with hands and arms; and talk or hear. The employee must lift and move up to 50 pounds.The noise level for this work environment is usually moderate.In keeping with its access, excellence and impact mission, The University of Texas at El Paso is committed to an open, diverse, and inclusive learning and working environment that honors the talents, respects the differences, and nurtures the growth and development of all. We seek to attract faculty and staff who share our commitment.The University of Texas at El Paso is an Equal Opportunity / Affirmative Action Employer. The University does not discriminate on the basis of race, color, national origin, sex, religion, age, disability, genetic information, veteran status, or sexual orientation and gender in employment or the provision of services in accordance with state and federal law. Discrimination on the basis of sex includes an employee's or prospective employee's right to be free from sexual harassment under Title IX of the Higher Education Amendments of 1972.For accommodation information for employees and applicants with disabilities, please contact UTEP's Equal Opportunity Office at <a href="mailto:eoaa@utep.edu.To" target="_blank">mailto:eoaa@utep.edu.To</a> apply, visit <a href="https://apptrkr.com/6140871jeid-4404a16562947c4399961c10fe17a78a" target="_blank">https://apptrkr.com/6140871jeid-4404a16562947c4399961c10fe17a78a</a>

The University of Texas at El Paso

Enterprse Desktop Mgmnt Spclst

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Traditional targets and modalities that have historically provided rich opportunities for drug discovery and decades of productive academic and industrial research are gradually giving way to new scientific frontiers. A steady shift is underway in the target and modality landscape, with novel approaches such as targeted protein degradation emerging as particularly exciting and rapidly evolving areas of research.We seek exceptional scientists who are high-energy, innately curious self-starters with versatile skill sets and the capacity to thrive in a dynamic, fast-paced research environment. Joining the New Leads and Computational Sciences team, you will drive our Protein Homeostasis portfolio by leveraging structure-based and ligand-based computational chemistry methods, data visualization, data analysis, and advanced machine learning and AI techniques. Your goal will be to design molecules demonstrating superior degradation profiles and pharmacological properties.In close collaboration with multidisciplinary Protein Degrader project teams, you will proactively generate and test scientific hypotheses, design and execute sophisticated computational experiments, deliver thorough analyses, interpret experimental outcomes, and translate insights into actionable molecular designs that meaningfully advance our discovery programs. Your technical expertise, clear communication skills, and collaborative approach will enable you to effectively partner with scientists across the R&amp;D organization, significantly influencing the pipeline from target identification through degrader optimization to candidate nomination.Responsibilities will include, but are not limited to, the following:<ul><li>Lead and influence the strategic application of computational methods to rigorously evaluate therapeutic targets, protein degradation modalities, and novel degrader designs within multidisciplinary project teams.</li><li>Develop and apply a diverse suite of computational chemistry methods to optimize molecules for potency, selectivity, protein degradation efficiency, and favorable ADME properties, while proactively identifying and mitigating potential toxicological risks.</li><li>Partner closely with experimental and project scientists to drive informed decision-making, ensuring computational insights directly support and accelerate project objectives.</li><li>Utilize structural modeling, artificial intelligence (AI), machine learning (ML), statistical analysis, and data visualization techniques to deepen structure-activity relationship (SAR) insights, contributing actively to project strategy and decision-making processes.</li><li>Innovate and apply advanced multi-parameter optimization approaches to identify and enhance biologically relevant molecular features, ensuring optimal therapeutic profiles.</li><li>Provide strategic scientific leadership in target validation and assessment activities, including comprehensive literature and patent reviews, competitive intelligence gathering, chemical feasibility evaluations, and in-depth characterization of target druggability and binding site properties.</li><li>Maintain expertise and continually expand your proficiency in state-of-the-art computational chemistry methods, actively exploring and implementing emerging technologies to enrich and advance our discovery pipeline.</li></ul>Background Requirements:<ul><li>A completed Ph.D. in computational chemistry or a related field with strong application background as demonstrated by contributions to leading journals</li><li>A minimum of 5+ years of biotech/pharmaceutical industrial experience.</li><li>Demonstrated expertise in a subset of computational methods, such as: docking methods, structure-based drug design, ligand-based drug design, molecular dynamics simulations, homology modeling approaches, free energy simulations, machine learning techniques, statistical methods, large-scale data visualization/analysis, molecular matched pair analyses, or multiple parameter optimization methods.</li><li>Demonstrated experience applying computational chemistry methods to a variety of biological targets (e.g., proteins, DNA, RNA). Familiarity with diverse therapeutic modalities is preferred, such as: covalent/non-covalent inhibitors, allosteric modulators, targeted protein degraders, antibodies, antibody-drug conjugates, etc.</li></ul> Scientific/Technical/Functional Skills:<ul><li>Proven expertise in computer-assisted drug design, proficiently utilizing industry-standard modeling and computational chemistry software tools.</li><li>Ability to independently review scientific literature and project data, creatively formulate design hypotheses, conduct insightful data analyses, and design innovative molecular agents tailored to project goals.</li><li>Demonstrated ability to serve as an independent computational chemist on discovery teams, proactively driving projects and ensuring timely achievement of scientific milestones.</li><li>Solid working knowledge of medicinal chemistry principles and drug discovery processes.</li><li>Familiarity with at least one scripting or programming language (e.g., Python, R, Java, C++).</li><li>Strong interpersonal, organizational, and communication skills, with a collaborative mindset that thrives in multidisciplinary and geographically dispersed project teams.</li><li>Scientific integrity, curiosity, creativity, proactive problem-solving abilities, and a high degree of motivation and work ethic.</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb

Senior Scientist, Next Generation Medicine Design

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.The Oncology Thematic Research Center at BMS is a key research and early development engine, responsible for the discovery and development of novel oncology therapeutics for patients.&nbsp; Centered at our state-of-the-art research sites in Cambridge and Seattle, scientists focus on novel targets and pathways for tumors that are refractory to current therapies.&nbsp; With a deep understanding of the causal human biology, we are able to leverage our multiple modality platforms to best match the modality to the mechanism and desired outcome.&nbsp; We are a fully integrated drug discovery through translational and early clinical development organization which exploits state-of-the-art in vitro, in vivo and ex-vivo models of Cancer biology and Immuno-oncology to identify and validate targets.&nbsp; &nbsp;We partner closely with colleagues in Translational Medicine, Informatics and Predictive Sciences and Early Clinical Development to generate biomarker and patient enrichment hypotheses to enable efficient decision making in early clinical trials.&nbsp; We are&nbsp;optimally positioned to complement the world-class translational expertise, biology and leading academic research centers in the area.Our Bristol Myers Squibb research site in Cambridge Crossing will help us continue to deliver on our mission, positioning the company and our scientists in the heart of a vibrant ecosystem of world-class science, innovation, and business opportunities.Position Summary:We are seeking an experienced individual with oncology discovery and/or translational expertise to join the Translational Research team within the Oncology Thematic Research Center at Bristol Myers Squibb in Cambridge, MA. The qualified candidate is a highly motivated, interactive, and creative scientist that can work across a highly matrixed organization to advance programs from candidate optimization through IND enabling activities and ultimately to Clinical Proof of Concept studies.&nbsp; This individual will be dedicated to designing scientific studies and delivering data that impact clinical decision-making for our programs.&nbsp; The candidate will explore patient stratification, drug combination, and/or biomarker concepts and execute bench studies that delivering data for Oncology TRC programs.Position Responsibilities:In the role as a Senior Scientist within Oncology Translational Research, the ideal candidate will:<ul><li>Develop biomarker, pharmacodynamic and target engagement assays.</li><li>Use current and new techniques to address drug mechanism of action and sensitivity/resistance studies.</li><li>Familiarity with various in vitro oncology models/assays in order to explore drug combination studies and indication selection.</li><li>Apply functional genomics tools (i.e. CRISPR, RNAi, ORF, etc.) in order to characterize oncogenic targets and drug mechanistic studies.</li><li>Familiarity with targeting tumor intrinsic vulnerabilities and RAS biology is highly desired.</li><li>Interact with project teams and contract laboratories for design and oversight of molecular, cellular and/or in vivo studies.</li><li>May be responsible for co-authoring non-clinical pharmacology study reports and scientific publications.</li><li>Expected to understand departmental goals and development processes.</li><li>Execute experiments independently, troubleshoot as needed, interpret and discuss data.</li><li>Utilize excellent communication and interpersonal skills.&nbsp; Communicate via email, meetings and reports.</li></ul>Experience =Basic Qualifications:<ul><li>Bachelor’s Degree<ul><li>7+ years of academic and / or industry experience</li></ul></li></ul>Or<ul><li>Master’s Degree<ul><li>5+ years of academic and / or industry experience</li></ul></li></ul>Or<ul><li>Ph.D. or equivalent advanced degree in the Life Sciences<ul><li>2+ of academic and / or industry experience</li></ul></li></ul>Preferred Qualifications:<ul><li>Ph.D. with post-doctoral experience and/or 1-3 years of industry experience, is highly desired.&nbsp; BA or MA with at least 5-7 years of industry experience in drug discovery or translational research in the pharma or biotech setting may be considered.</li><li>Experienced in the design and development of cell-based assays using various technology platforms, especially generation and characterization of patient-derived material including organoid or tumoroid cultures and ex vivo manipulation and propagation is highly valued but not required</li><li>Experience performing laboratory work, including handling cell cultures and performing analysis of protein and DNA/RNA samples using a variety of methodologies including but not limited to: flow cytometry, MSD/ELISA, Luminex, RNAi, CRISPR, qPCR and primary cell isolation, culture and functional assays.</li><li>Ability to conduct experimental work independently, with accurate, detailed record-keeping.</li><li>Ability to efficiently manage and prioritize multiple projects, coordinating in-house research with collaborative work.</li><li>Ability to summarize and interpret scientific data in a clear, concise, and accurate manner.</li><li>Excellent oral and written communication skills.&nbsp; Ability to communicate well with peers and supervisors.</li><li>Strong problem-solving skills and understanding of relevant scientific principles.</li><li>Ability to be flexible in case of changing priorities.</li></ul>#LI-OnsiteIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior Scientist, Translational Research

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position Summary<ul><li>Responsible for design and execution of assigned clinical trial activities and works closely with clinical team members to execute activities associated with trial conduct.</li></ul><ul><li>May lead or support trial level activities for one or more trials with the necessary supervision.</li></ul>Duties/Responsibilities&nbsp;<ul><li>Collaborate and liaise with external partners (e.g., KOLs).</li></ul><ul><li>Seek out and enact best practices with instruction.&nbsp;&nbsp;</li></ul><ul><li>Provide regular and timely updates to manager/management as requested.&nbsp;</li></ul><ul><li>Collaborate cross-functionally to develop Protocol and ICF documents / amendments and present these to governance committee and early clinical development team meetings as required.&nbsp;&nbsp;</li></ul><ul><li>Conduct literature review.&nbsp;</li></ul><ul><li>Develop site and CRA training materials and present these at SIVs and Investigator meetings.&nbsp;&nbsp;</li></ul><ul><li>Review clinical narratives.&nbsp;&nbsp;</li></ul><ul><li>Collaborate cross-functionally to monitor clinical data for specific trends.&nbsp;&nbsp;</li></ul><ul><li>Contribute to the development of Data Review Plan in collaboration with Data Management.&nbsp;</li></ul><ul><li>Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming.&nbsp;&nbsp;</li></ul><ul><li>Author/review clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., Pre-IND, IND, IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.)&nbsp;</li></ul><ul><li>Submit clinical documents to TMF.</li></ul>Reporting RelationshipDirector, Clinical Science Early Clinical Development (HOCT)QualificationsSpecific Knowledge, Skills, Abilities:<ul><li>Basic planning/project management skills (develop short range plans that are realistic and effective).</li></ul><ul><li>Basic knowledge of disease area, compound, current clinical landscape.&nbsp;&nbsp;</li></ul><ul><li>Detail-oriented with commitment to quality</li></ul><ul><li>Intermediate critical thinking and problem-solving skills.&nbsp;&nbsp;</li></ul><ul><li>Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism).</li></ul><ul><li>Intermediate skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., patient profiles, report generating tools).</li></ul>Education/Experience/ Licenses/Certifications:&nbsp;<ul><li>Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field preferred).</li></ul><ul><li>Expectation of 2+ years of experience in clinical science, clinical research, or equivalent.&nbsp;</li></ul><ul><li>Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.&nbsp;</li></ul><ul><li>Ability to understand assigned protocol(s) and their requirements.&nbsp;</li></ul><ul><li>Knowledge and skills to support program-specific data review and trend identification.&nbsp;</li></ul><ul><li>Intermediate medical writing skills and medical terminology.&nbsp;</li></ul><ul><li>Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees.</li></ul>Travel:<ul><li>Domestic and International travel may be required (10 - 25%).</li></ul>The starting compensation for this job&nbsp;is a range from $150,770- 201,000, plus incentive cash and stock opportunities (based on eligibility).The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed.Final, individual compensation will be decided&nbsp;based on demonstrated&nbsp;experience.&nbsp;Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit <a href="https://careers.bms.com/life-at-bms/" target="_blank">https://careers.bms.com/life-at-bms/</a>.Benefit&nbsp;offerings&nbsp;are subject to the terms and conditions of the applicable plans then in effect&nbsp;and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support&nbsp;such as&nbsp;the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support.&nbsp;Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility.&nbsp;Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Clinical Scientist, Early Clinical Development

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.The Neuroscience TRC is committed to the development of transformational therapeutics for patients with neurodegenerative, neuropsychiatric and neuromuscular diseases. A network of external partnerships paired with internal discovery of small molecules, biologics and genetic medicines supports our ambition to become leaders in neuroscience. Internal research focuses on causal human biology linking the immune system, protein clearance and synaptic mechanisms with nervous system disorders, applying human cells, AI, ML and high-throughput biology to identify and validate novel mechanisms.Areas of interest include, but are not limited to, the identification of disease modifying and symptomatic therapies for neurodegenerative, neuropsychiatric, neuroinflammatory and neuromuscular diseases; approaches to modulate protein clearance and reduce or eliminate toxic protein production; emerging technologies (RNA, DNA targeting) that when matched to underlying causal human biology may deliver a precision medicine portfolio with a high probability of translational success. We emphasize identification of neuroimaging and fluid biomarkers to track disease progression, target engagement and therapeutic response in our discovery and clinical programs.Position Summary: The Neuroscience Thematic Research Center (Neuro TRC) leverages external collaborations and internal research to establish a diverse portfolio targeting unmet needs in neurodegenerative, neuropsychiatric, neuroinflammatory and neuromuscular, diseases.The Senior Associate Scientist, Translational Discovery, in collaboration with other members of the Neuro TRC, undertakes design and delivery of translational data packages that enable rapid progression of drug candidates towards clinical proof-of-concept. This position is based in Cambridge, MA, and is primarily a laboratory-based role.Position Responsibilities:In the role as a Senior Associate Scientist within the Translational Discovery group, the ideal candidate will:<ul><li>Work closely with the team to develop target engagement and biomarker assays for assets in early development.</li><li>Drive biomarker assay qualification with CROs.</li><li>In collaboration with Global Biospecimen Inventory Management, manage TRC specimens for target engagement and biomarker development</li><li>Prepare data packages to support target engagement and biomarker data inclusion for phase 1 studies.</li><li>Work closely, in collaboration with in-house science teams, on study designs, data analyses, interpretation that support high priority neuro projects/programs.</li><li>Draft and review internal project reports as needed; present scientific data at internal and external conferences.</li></ul>Experience = Basic Qualifications: <ul><li>Bachelor’s Degree<ul><li>4+ years of academic and / or industry experience</li></ul></li></ul>Or<ul><li>Master’s Degree<ul><li>2+ years of academic and / or industry experience</li></ul></li></ul>Preferred Qualifications: <ul><li>Hands on experience in immunoassay and molecular assays (ELISA, Meso-scale discovery, SIMOA, qPCR, dd-PCR, RNAseq, etc.).</li><li>Experience in managing biorepositories</li><li>Proven track record in designing, troubleshooting, analyzing and interpreting data from translational and experimental medicine type studies.</li><li>Experience transferring assay to contract research organizations for analysis in multi-site clinical trials.</li><li>Deep understanding of unmet need and clinical outcome measures used in studies focused on neurodegenerative disorders</li><li>Excellent oral and written communication skills</li><li>Ability to work both independently and as a well-integrated member of multidisciplinary drug development teams</li></ul>#LI-OnsiteIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior Associate Scientist, Neuroscience Translational Discovery

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.<h4>Title: Medical Science Liaison, Neuropsychiatry </h4><h4>Location: West Texas (Austin/San Antonio/El Paso, New Mexico)</h4>The Medical Science Liaison (MSL) role embodies our medical mission to be recognized as the trusted partner for internal stakeholders and the&nbsp;healthcare community, driving scientific exchange to enhance medical education, data generation, insight generation and patients’ access to medicine.The MSL is responsible for identifying disease and product related medical needs in a defined geography. The primary role of the MSL is to develop and maintain relationships with Thought Leaders (TL) and Healthcare Providers (HCP) within their territory. The purpose of their interactions is to engage in meaningful scientific exchange that will ensure patients have access to BMS medicines, to ensure their safe and appropriate use through peer-to-peer discussions aligned with medical strategies and needs expressed by external stakeholders, and to facilitate research. The MSL also serves as the medical resource for external stakeholders in the community.ExternalEnvironmentandCustomerFocus<ul><li>Develop and maintain relationships with academic and community research thought leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product, and Health Economics and Outcomes Research (HEOR)-related questions. The MSL will use various channels for interactions (1:1, group presentations, remote, etc.)</li><li>Demonstrate proficiency in using available scientific resources and presentations. Effectively present information to TLs/HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives.</li><li>Actively assess the medical landscape by meeting with TLs/HCPs/Access Stakeholders to understand their needs and expertise. Continuously update their own knowledge in treatment strategies, products, unmet medical needs, clinical trials, health economics outcomes research and scientific activities. Understand the competitive landscape and evolving healthcare models and actively prepare to address informational needs of customers</li><li>Identify opportunities to partner with HCPs on disease state initiatives, collaborative research projects, and investigator sponsored research (ISR) of interest and in alignment with BMS strategic objectives</li><li>Attend medical congresses and local/regional meetings. Collect and provide meaningful medical insights and/or impact by communicating these back to the medical and commercial organizations to support strategy development and business decisions</li></ul>Contribute to the Medical Plan<ul><li>Develop geography-specific Field Medical and TL Interaction plans based on therapeutic area objectives and TLs needs</li><li>Adopt institution/account planning approach and contribute to cross-functional institution/account plans</li><li>Contribute to development and delivery of scientifically meaningful medical programs/projects in line with the local Medical and Field Medical plan</li></ul>Provide Medical Support<ul><li>Establish a customer-centric, compliant collaboration with cross-matrix field teams within assigned geography</li><li>As necessary and appropriate, support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (e.g. Commercial, Regulatory, Pharmacovigilance, Legal, HEOR, Value Access &amp; Payment)</li><li>Provide scientific support at promotional meetings by presenting scientific and clinical data, by evaluating speakers and by giving support to BMS-contracted speakers (if applicable)</li><li>Participate in assigned Congress activities</li></ul>Support Clinical Trial Activities<ul><li>Support Interventional and Non-Interventional Research (NIR) studies (e.g. identification and assessment of potential study sites) to facilitate patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with home office medical and Global Development Operations (GDO) and as defined by the study scope document</li><li>Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with home office medical and GDO</li><li>Support HCPs in the ISR submission and execution process and study follow-up as agreed upon with home office medical and GDO</li><li>Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events</li><li>Actively support CRO sponsored studies as agreed with home office medical and GDO and as defined by the study scope document</li></ul>Required Qualifications<ul><li>Advanced degree in medical/biosciences (i.e., MD, PhD, PharmD, DPH, EdD, etc.) AND a minimum 3-5 years of MSL or clinical practice experience</li><li>Current MSL or clinical practice experience in psychiatry, mental health or schizophrenia with proven track record of establishing, maintaining, and enhancing effective and successful collegial relationships with external experts.</li></ul>Knowledge Desired<ul><li>Disease area knowledge and an understanding of scientific publications</li><li>Knowledge of a scientific or clinical area, competitive landscape and patient treatment trends</li><li>Knowledge of clinical trial design and process</li><li>Knowledge of the national healthcare and access environment</li><li>Knowledge of HEOR core concepts</li><li>Excellent English language skills, spoken and written</li></ul>Experience Desired<ul><li>A minimum of 2 years working in a clinical and/or pharmaceutical environment</li><li>Prior MSL or clinical practice experience</li><li>Ability to work independently and act as a team player</li><li>Translating scientific or clinical data into an understandable and valuable form to help physicians best serve their patients</li><li>Good communication and presentation skills to present scientific and/or clinical data to research or healthcare professionals</li><li>Developing peer-to-peer relationships with TLs, scientists and other HCPs</li><li>Ability to quickly and comprehensively learn about new subject areas and environments</li><li>Demonstration of the BMS Values</li></ul>Essential Qualification<ul><li>Ability to drive a company-provided car is an essential qualification of this position. Candidates must be able to drive a BMS-provided vehicle between locations (often great distances apart) and arrive at each location ready and able to enthusiastically and efficiently demonstrate an applied knowledge of pertinent health care industry trends. Candidates must possess a high level of ethics, integrity, and a responsible and safe driving history.</li></ul>Travel Requirement<ul><li>Travel required. This position is field based and the MSL will be required to live within the territory they manage or within 50 miles of the territory borders.</li><li>The MSL&nbsp;will spend the majority of their time in the field with external customers. Further requirements based on territory assignment and team needs.</li></ul>The starting compensation for this job is a range from $150,000 - $200,000, plus incentive cash and stock&nbsp;opportunities (based on eligibility).&nbsp;The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed.&nbsp;Final, individual compensation will be decided based on demonstrated experience.&nbsp;Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Careers site.&nbsp;Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical,&nbsp;pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP).&nbsp;Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental&nbsp;health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays,&nbsp;Global Shutdown days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick&nbsp;time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and&nbsp;surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like&nbsp;tuition reimbursement and a recognition program.&nbsp;#LI-RemoteIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Medical Science Liaison, Neuropsychiatry (West Texas)

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position Summary:Subject matter expert supporting method transfer/validation and routine testing of in-process, final product, and stability samples. Perform data review/verification, complex troubleshooting, and method training. Own project, document revisions, deviations/investigations/CAPA, and continuous improvement efforts.Duties/Responsibilities:<ul><li>Subject matter expert supporting method transfer/validation and routine testing of in-process, final product, and stability samples.</li><li>Perform review of testing data (e.g., data packets, final lot file, COA review).</li><li>Anticipate and perform complex troubleshooting and problem-solving independently.</li><li>Perform data verification, data review, and review of GMP documentation for multiple methods (general and complex) and/or products.</li><li>Own project, CAPA, and deviation/investigation-related tasks and/or continuous improvement efforts.</li><li>May represent the department in regulatory inspections (internal and external audits).</li><li>Train and mentor others on multiple QC test methods, processes, and procedures.</li><li>Cross-trained on multiple complex analytical methods and/or multiple products.</li><li>Author and review/revise technical documents such as test methods, SOPs, specifications, trend reports, and/or sample plans as appropriate.</li><li>Perform other tasks as assigned.</li></ul><h4>Qualifications</h4><h4>Specific Knowledge, Skills, and Abilities:</h4><ul><li>Ability to accurately and completely understand, follow, interpret, and apply Global Regulatory and cGMP requirements.</li><li>Demonstrated technical writing skills.</li><li>High problem-solving ability/mentality, technically adept, and logical.</li><li>Ability to communicate effectively with peers, department management, and cross-functional peers about task status, roadblocks, and needs.</li><li>Advanced ability to work in a fast-paced team environment, meet deadlines, and prioritize work from multiple projects.</li><li>Advanced knowledge of LIMS, ELN, and laboratory data analysis systems preferred.</li><li>Strong mentoring, coaching, influencing, negotiating, and personnel interaction skills.</li></ul><h4>Education/Experience/Licenses/Certifications:</h4><ul><li>Bachelor’s degree or equivalent required, preferably in science. Advanced degree preferred.</li><li>Netherlands: PhD in (bioanalytical) science preferred. Bachelor's degree in (bioanalytical) science with an equivalent combination of work experience may be considered.</li><li>6+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.</li><li>Demonstrated experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, ELISA, and aseptic technique).</li></ul>BMSCART#LI-OnsiteIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Scientist, QC Analytical, Cell Therapy

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.RayzeBio, a Bristol Myers Squibb company, is seeking applicants for an Environmental Monitoring Technician. Reporting to the QC Microbiology Manager, the Environmental Monitoring Technician will help support the contamination control and sterility assurance activities for the controlled environments at the manufacturing facility in Indianapolis. This role will conduct environmental monitoring of aseptically produced targeted alpha therapy (TAT) radiopharmaceuticals for RayzeBio’s clinical and commercial programs.Job ResponsibilitiesEssential duties and responsibilities include the following:<ul><li>Perform routine environmental monitoring of cleanrooms such as viable airborne monitoring, non-viable particulate sampling, and viable surface monitoring.</li><li>Support aseptic manufacturing activities such as media fills, personnel sampling, etc.</li><li>Ensure the use of proper aseptic techniques and compliance with SOPs during monitoring of controlled environments and utility systems.</li><li>Prepare sample data, results, reports and other documents that are generated from environmental monitoring activities</li><li>General laboratory housekeeping duties and maintenance of the department and equipment.</li><li>Assist in stocking and organizing lab consumables required for environmental monitoring and microbiology testing.</li><li>Read plates to quantify microbial growth and subculture pure isolates as required.</li><li>Support and provide technical, quality, and/or safety information pertaining to environmental monitoring tests to lab management on routine basis.</li><li>Participate in troubleshooting and investigations of environmental excursions to identify root causes and implement corrective actions as required.</li><li>Ensure compliance with GMP regulations, radiation safety guidelines, and quality standards.</li><li>Perform other duties as required by management.</li><li>Generally first shift (6:00 AM-2:30 PM) Monday-Friday, but extended hours or weekend work based on radiopharmaceutical manufacturing schedule may be required.</li></ul>Education and Experience:<ul><li>Associate or bachelor’s degree in biology, Microbiology, or other Life Science related field and 0-1 years of relevant experience in production or quality control in a cGMP/FDA regulated facility.</li><li>A high school diploma may be acceptable with sufficient prior cleanroom and/or environmental monitoring experience in a cGMP/FDA regulated facility</li><li>Experience with sterile manufacturing and/or radiopharmaceuticals preferred.</li></ul>Skills and Qualifications<ul><li>Highly motivated and organized individual with the ability to work both independently and in a team environment.</li><li>Ability to multi-task and prioritize work based on multiple workflows.</li><li>Strong written and verbal communication skills required.</li><li>Excellent professional ethics, integrity, and ability to maintain confidential information.</li><li>Work with computer programs, including but not limited to Microsoft Office.</li></ul>Physical DemandsWhile performing duties of this job, the employee is regularly required to stand, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 40 pounds. Specific vision abilities required by this job include close vision. The employee must be comfortable gowning in PPE for extended periods of time to work in a cleanroom environment and working in manufacturing and laboratory environments ionizing radiation, biohazardous materials, and hazardous chemicals.Work EnvironmentThe noise level in the work environment is usually moderate.#RayeBio, #LI-OnsiteIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Technician, Environmental Monitoring - Microbiology

Job Title Laboratory Scientist/Certified/UKHC Requisition Number RE49907 Working Title Laboratory Scientist Certified - Stem Cell Department Name H3200:Laboratory Services Work Location Lexington, KY Grade Level 11 Salary Range $26.00-45.70/hour Type of Position Staff Position Time Status Full-Time Required Education BS Click here for more information about equivalencies: <a href="https://hr.uky.edu/employment/working-uk/equivalencies" target="_blank">https://hr.uky.edu/employment/working-uk/equivalencies</a> Required Related Experience No experience required. Required License/Registration/Certification Certification Physical Requirements This position will require the ability to stand and walk for long periods of time as well occasionally standing or walking with objects up to 10 pounds and push or pull objects over 50 pounds. Shift Mainly day shift from 10a-630p with shift flexibility dependent on patient flow and department need. Occasional weekends. May include call based on needs of the department. Job Summary The Laboratory Scientist/Certified/UKHC will be responsible for performing laboratory testing in a fast-paced academic medical center. The Laboratory provides services to all aspects of the Level I trauma center and throughout the healthcare enterprise, including solid organ and bone marrow transplant, KY Children’s Hospital, and Markey Cancer Center. This position, located in the Cell Therapy Lab, will process, evaluate, preserve, store, and thaw cell therapy products vital to hemopoietic stem cell transplant patient recovery and survival. Cell therapy products include bone marrow, peripheral blood stem cells, and therapeutic cells. The Laboratory Scientist will be expected to function within compliance standards and have a high quality approach. This position will also provide excellent customer service to all internal and external customers and have the ability to help update and evolve the procedures within the laboratory. This CAP and FACT Accredited Laboratory at the University of Kentucky utilizes good tissue practice (GTP). The Laboratory Services department has a variety of specialties and areas. For additional information regarding the Laboratory Services department, please follow the link to view a departmental video. IMPORTANT: Resumes and CVs cannot be substituted for a completed application. Incomplete applications could disqualify you from being considered for this position. To be considered for this position you must fully complete the online application being sure to only put one (1) job title for each entry (multiple job titles for one employer must have separate entries), the # of hours worked per week and your ending salary. All job titles and dates must correspond with those appearing on your resume. Skills / Knowledge / Abilities Exceptional customer service, excellent technical skills, detail oriented, and collaboration skills with different positions across the hospital. Other skills include Microsoft Office knowledge and proficient writing ability, hospital electronic systems, knowledge of medical terminology, and ability to work independently as well as part of a team. Does this position have supervisory responsibilities? No Preferred Education/Experience Three or more years of experience in a clinical laboratory preferred. Knowledge of hematology, immunology, and/or blood banking, including processing and/or cryopreservation concepts and practices preferred. Deadline to Apply 04/23/2025 Our University Community We value the well-being of each of our employees and are dedicated to creating a healthy place for everyone to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors the University of Kentucky is a Tobacco &amp; Drug Free campus. As an Equal Opportunity Employer, we strongly encourage veterans, individuals with disabilities, women, and all minorities to consider our employment opportunities. Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen.

Laboratory Scientist/Certified/UKHC

<h4>Thanks for your interest in Children's Mercy!</h4>Do you envision finding a meaningful role with an inclusive and compassionate team? At Children’s Mercy, we believe in making a difference in the lives of all children and shining a light of hope to the patients and families we serve. Our employees make the difference, which is why we have been recognized by U.S. News &amp; World Report as a top pediatric hospital, for eleven consecutive years.Children’s Mercy is in the heart of Kansas City – a metro abounding in cultural experiences, vibrant communities and thriving businesses. This is where our patients and families live, work and play. This is a community that has embraced our hospital and we strive to say thanks by giving back. As a leader in children’s health, we engage in meaningful programs and partnerships throughout the region so that we can improve the lives of children beyond the walls of our hospital.<h4>Overview</h4>The Principal Data Scientist is responsible for delivering data science and Artificial Intelligence (AI) projects for Acute Care and Inpatient Operations, aligning data science initiatives with the priorities of our organization, and collaborating with clinical and operational leaders to drive data-driven decision-making in alignment with our strategic goals. Reporting to the Chief Data Officer, the Principal Data Scientist plays a pivotal role for the AI Center of Excellence (The AI IDEA Lab), assisting in efforts to build a strategic roadmap for AI at Children's Mercy, as well as assisting with AI governance processes and standards. Principal has mentorship responsibilities, assisting other Children's Mercy team members by communicating best practices in advanced analytics, data science, and machine learning.At Children’s Mercy, we are committed to ensuring that everyone feels welcomed within our walls. A successful candidate for this position will join us as we strive to create a workplace that reflects the community we serve, as well as our core values of kindness, curiosity, inclusion, team and integrity.Additionally, it’s important to us that we remain transparent with all potential job candidates. Because we value the safety of the patients and families we serve, as well as the Children’s Mercy staff, we want to let you know that the seasonal influenza vaccine is a condition of employment for all employees in our organization. New employees must be willing to be vaccinated if found non-immune to measles, mumps, rubella (MMR) and chicken pox (varicella) and/or without evidence of tetanus, diphtheria, acellular pertussis (Tdap) vaccination since 2005. If you are selected for this position, you will be asked to supply your immunization records as proof of vaccination. If you and have any concerns about receiving these vaccines, medical and/or religious exemptions can be further discussed with Human Resources.<h4>Responsibilities</h4>Develop, deploy, and maintain complex algorithms, in support of Acute Care and Inpatient Operations, resulting in insightful output that integrates with our Patient Progression Hub (and other systems), through the use of our data platform technologies:•&nbsp;Design, develop, and implement algorithms to analyze complex healthcare data, providing actionable insights to guide operational strategy and improve patient outcomes.•&nbsp;Utilize advanced machine learning techniques to perform in-depth analysis of healthcare and/or operational data, identifying patterns and insights to improve patient outcomes.•&nbsp;Work with leaders, stakeholders, and collaborators to proactively identify desired clinical and/or operational outcomes associated with a given data science project.•&nbsp;Collaborate with cross-functional teams to integrate model outputs with existing systems and workflows, ensuring seamless data flow and utilization.•&nbsp;Ensure scalability and reliability of analytical output by utilizing our cloud-based data platform (as well as other software solutions and data science tools) to explore large, complex data sets, as well as to&nbsp; &nbsp; manage and deploy models.•&nbsp;Explain complex and technical details to non-technical collaborators, ensuring accurate and mutual understanding of the underlying context of a project, as well as the resulting insights of each analytical endeavor.•&nbsp;Develop and deploy enterprise-level, production-grade, and impactful machine learning products by way of maintainable code, automated testing, and CI/CD processes.•&nbsp;Ensure all data handling and analysis practices comply with ethical standards and regulations, prioritizing patient confidentiality, data security, and the responsible use of sensitive pediatric health information.Provide leadership in building and sustaining a robust, enterprise-wide strategy for utilizing Artificial Intelligence at Children's Mercy:•&nbsp;Partner with other members of the AI IDEA Lab to develop organization-wide standards and best practices for the development, deployment, and management of AI solutions.•&nbsp;Continually seek and coordinate opportunities for collaboration and knowledge sharing amongst AI and data science stakeholders at Children’s Mercy.•&nbsp;Regularly review scientific literature, attend conferences, and participate in educational opportunities to stay updated on the latest advancements in data science and AI, particularly those relevant to pediatric healthcare.•&nbsp;Assess emerging data science tools and AI technologies for potential integration into hospital systems, ensuring they meet the specific needs of pediatric care.Provide guidance to leaders, engineers, and data scientists to drive the design, development, and adoption of data science solutions:•&nbsp;Mentor less experienced team members and provide coaching as needed.•&nbsp;Prepare content for inclusion in publications and public presentations by articulating clear depictions of methodologies, interpretation of results, and effective design of data visualizations.•&nbsp;In partnership with other Data Intelligence team members, develop and deliver AI literacy content to stakeholders across Children’s Mercy.•&nbsp;Provide consultation to other technologists and leaders on emerging best practices in data science and analytics solution development.<h4>Qualifications</h4><ul><li>Ph.D. in Data Science, or related area of study, and 6+ years in health care analytics or data science OR</li><li>Master's Degree in Data Science or related area of study and 8+ years in health care analytics or data science OR</li><li>Bachelor's Degree in Data Science or related area of study and 10+ years in health care analytics or data science.</li></ul> <h4>Benefits at Children's Mercy</h4>The benefits plans at Children’s Mercy are one of many reasons we are recognized as one of the best places to work in Kansas City. Our plans are designed to meet the changing needs of our employees and their families. Learn more about Children’s Mercy benefits. <h4>Starting Pay</h4>Our pay ranges are market competitive. The pay range for this job begins at $64.48/hr, but your salaried offer will be determined based upon your education and experience.<h4>Remote Work/Work from Home</h4> This position is entirely remote or work from home. The person hired must live in the Kansas City metro area or request advanced approval to work outside of the area and may attend onsite meetings, as scheduled.<h4>EEO Employer/Disabled/Vet</h4>Children’s Mercy hires individuals based on their job skills, expertise and ability to maintain professional relationships with fellow employees, patients, parents and visitors. A personal interview, formal education and training, previous work experience, references and a criminal background investigation all are factors used to select the best candidates. The hospital does not discriminate against prospective or current employees based on the race, color, religion, sex, national origin, age, disability, creed, genetic information, sexual orientation, gender identity or expression, ancestry or veteran status. A drug screen will be performed upon hire. Children’s Mercy is smoke and tobacco free.<h4>Our commitment to Diversity &amp; Inclusion</h4>CM is committed to creating a diverse and inclusive workforce. Our patients and families come from all walks of life, and so do we. We know that our greatest strengths come from the people who make up our team so we hire great people from a wide variety of backgrounds, not just because it’s the right thing to do, but because it makes our hospital stronger and our patient care more compassionate.If you share our values and our enthusiasm for service, you will find a home at CM. In recruiting for our team, we welcome the unique contributions that you can bring, including education, ideas, culture, ethnicity, race, sex, sexual orientation, gender identity and expression, national origin, age, languages spoken, veteran status, color, religion, disability and beliefs.<h4>Need help finding the right job?</h4>We can recommend jobs specifically for you!Click here to get started.

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