Join as Clinical Scientist at Bristol Myers Squibb! Apply Now!

Bristol Myers Squibb invites applications for a Clinical Scientist position in Immunology, based at Princeton and Madison (Giralda), NJ. This hybrid role offers a unique opportunity to be part of groundbreaking clinical research programs that transform lives. If you have a degree in life sciences and a passion for clinical trials and scientific innovation, join BMS to advance your career in a dynamic and meaningful environment.

About the Company:

Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a focus on cutting-edge science and a dedication to improving lives, BMS provides meaningful career opportunities across a wide range of disciplines. Their culture promotes balance, flexibility, and the pursuit of both professional and personal goals. At BMS, every role is essential in transforming lives through science and innovation.

Job Details: 

• Position: Clinical Scientist – Immunology
• Location: Princeton, NJ & Madison (Giralda), NJ (Hybrid)
• Employment Type: Full-time, Hybrid

Position Summary / Objective

• Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct

• May serve as Clinical Trial Lead for one or more trials

• May lead or support trial level activities for one or more trials with the necessary supervision

• May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members

Position Responsibilities

• Collaborate and liaise with external partners (e.g., KOLs)

• Seek out and enact best practices with instruction

• Provide regular and timely updates to manager/management as requested

• Develop Protocol and ICF documents/amendments and present these to governance committee and development team meetings as required

• Conduct literature review

• Submit clinical documents to TMF

• Develop site and CRA training materials and present these at SIVs and Investigator meetings

• Review clinical narratives

• Monitor clinical data for specific trends

• Develop Data Review Plan in collaboration with Data Management

• Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming

• Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.)

Degree Requirements

Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred).  Appropriate for new entrance to pharma (post fellowship/ new to industry)

Experience Requirements

• Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations

• Ability to understand assigned protocol(s) and their requirements

• Basic knowledge skills to support program-specific data review and trend identification

• Intermediate medical writing skills and medical terminology

• Basic planning/project management skills (develop short range plans that are realistic and effective)