
location_onPeabody Street, Neighborhood Nine, Cambridge, Middlesex County, Massachusetts, 02318, United States
Challenging, meaningful, and life-changing work happens every day at Bristol Myers Squibb. From optimizing production lines to driving breakthroughs in cell therapy, our teams transform the lives of patients while advancing their own careers. We recognize the importance of balance and flexibility, offering a wide variety of competitive benefits and programs to support our employees in pursuing their goals both at work and in their personal lives.
With a vision to "Transform patients' lives through science," every employee plays an integral role in work that goes far beyond the ordinary. Our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of our colleagues, empowering individuals to apply their unique talents in a supportive culture that promotes global participation in clinical trials.
The Clinical Development Lead sits within Clinical Development, a global organization dedicated to the effective design and execution of drug development. This role serves as the clinical point of accountability for the Development Team, responsible for the overall clinical development plan for assets in one or more indications or tumor types. As a matrix leader, you will lead, develop, and motivate teams to achieve results, ensuring studies are aligned with target label indications and designed to meet regulatory, quality, medical, and access goals.
You will partner with Clinical Trial Physicians (CTPs) and Clinical Scientists to drive the clinical contribution to indication strategies, including registrational and non-registrational studies. This position requires a commitment to developing a resilient attitude, embracing change, and championing a quality-focused mindset to ensure adherence to Good Clinical Practice (GCP) and compliance obligations. You will represent Clinical Development in internal and external forums as the consulted authority for the disease area, collaborating with Key Opinion Leaders (KOLs) and serving as the primary clinical representative in regulatory interactions.
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.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process. Applicants can request reasonable workplace accommodations or adjustments prior to accepting a job offer. If you require accommodations during the application or recruitment process, please direct your inquiries to adastaffingsupport@bms.com.
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
We consider qualified applicants with arrest and conviction records pursuant to applicable laws. For candidates in Los Angeles County, additional information regarding employment rights is available on our careers site. We will never request payments, financial information, or social security numbers during our application or recruitment process.
Work model: On-site
Peabody Street, Neighborhood Nine, Cambridge, Middlesex County, Massachusetts, 02318, United States
Cambridge, Massachusetts
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Skills: Clinical Development Strategy, Clinical Trials, GCP, Regulatory Submission, Phase Ii-Iii Trials, First In Human, Proof Of Concept Trials, Target Product Profile, Risk Management Plan, Clinical Trial Physician.
Education: MD required with deep understanding of clinical principles.