Senior Manager, Global Clinical Scientist - Psychiatry

Challenging. Meaningful. Life‑changing. Working at Bristol Myers Squibb transforms patient lives and careers. Opportunities for growth, collaboration, and impact span across diverse departments. Position Summary / Objective Responsible for design and execution of assigned clinical trial activities. Work closely with clinical team members within the assigned project. May serve as Clinical Trial Lead for one or more trials. May lead or support trial‑level activities with appropriate supervision. May co‑lead study team meetings with the GDO protocol manager. Position Responsibilities Collaborate and liaise with external partners, including KOLs. Seek out and implement best practices. Provide regular and timely updates to manager/management. Develop protocol and ICF documents/amendments and present to governance committees and development team meetings. Conduct literature reviews. Submit clinical documents to TMF. Develop site and CRA training materials and present at SIVs and investigator meetings. Review clinical narratives. Monitor clinical data for trends. Develop data review plan in collaboration with Data Management. Ensure CRF design supports data collection in alignment with protocol in collaboration with Data Management/Programming. Submit clinical contributions to CSRs and the clinical portions of regulatory documents (IB, DSUR, PSUR, orphan reports, HA, EC, IRB responses). Contribute to regulatory submission. Degree Requirements Degree in Life Sciences (MD, PhD, PharmD, MS, RN or other scientific field). Preference for new entrants to pharma (post‑fellowship or new to industry). Experience Requirements Basic knowledge of GCP/ICH, drug development process, study design, statistics, and clinical operations. Ability to understand assigned protocol(s) and requirements. Skills to support program‑specific data review and trend identification. Intermediate medical‑writing skills and medical terminology. Basic planning/project‑management skills (develop realistic short‑range plans). Key Competency Requirements Detail‑oriented with commitment to quality. Basic knowledge of disease area, compound, and current clinical landscape. Knowledge of data monitoring committees, dose review teams, and independent response adjudication committees. Intermediate critical‑thinking and problem‑solving skills. Adaptable and flexible, able to adjust to multiple demands and shifting priorities. Intermediate proficiency in Microsoft Word/Excel/PowerPoint and data‑review tools. Travel Required Domestic and international travel may be required. Benefits Overview Health coverage: medical, pharmacy, dental, and vision. Well‑being programs and employee assistance. 401(k), disability, life insurance, and supplemental insurance. Paid time off, flexible time off, and additional leave options. Equal Employment Opportunity Bristol Myers Squibb is an equal opportunity employer. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, disability, veteran status, or any other protected category. #J-18808-Ljbffr Bristol Myers Squibb EU Policy