Clinical Scientist - Psychiatry (Sr Manager)

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. The Clinical Scientist role is essential for providing scientific expertise to design and deliver clinical studies and programs. This position involves leading and executing clinical trial activities, collaborating with cross-functional teams, and liaising with external partners such as Key Opinion Leaders (KOLs). Key responsibilities include developing and presenting protocol documents, conducting literature reviews, monitoring clinical data, and contributing to clinical study reports and regulatory submissions. Position Summary • 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 We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working. Supporting People with Disabilities