Bristol Myers Squibb · 2 hours ago
Clinical Development Lead Prostate (ACP3)
Bristol Myers Squibb is a dynamic biotechnology company focused on improving the survival of people with cancer. The Clinical Development Lead will design and lead clinical development plans targeting prostate cancer, providing medical direction and overseeing the execution of clinical trials.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Interact with clinical investigators and thought leaders to design a clinical development plan for nominated drug candidates
Lead internal project teams, and partner with investigators and CROs to design and implement clinical studies
Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and regulatory documents
Conduct investigator meetings and lead site qualification and initiation visits with clinical trial investigators
Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets
Translate findings from research and nonclinical studies into clinical development opportunities
Oversee Data Review and Independent Data Monitoring Committees
Conduct clinical trials using ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines
Establish and maintain positive relationships with clinical trial investigators and thought leaders
Serve as clinical lead for regulatory interactions, including preparation of briefing documents and attendance and presentation at health authority meetings
Supervise and mentor clinical scientists and medical directors
Willing to travel approximately 30% of the time
Qualification
Required
MD or equivalent with sub-specialty training in oncology and at least 8 years of pharmaceutical/biotech in oncology solid tumor clinical development
Drug development experience in GU cancer, prostate cancer, lung cancer or other solid tumor cancers is required
Patient-focused, with deep commitment to understanding needs and improving the lives of patients with cancers and a passion for developing novel therapeutics
Motivated to work in a fast-paced, high accountability, small company environment
Demonstrated record of accomplishment in a compressed time frame; capable of prioritizing tasks and delivering on deadlines with high performance standards and attention to detail
Demonstrated ability to collaborate successfully with multiple functions in a team environment
Intellectually curious with courage to challenge and seek new ways to improve work
Strong written and oral communication skills, including presentation skills
Ability to analyze and interpret data and develop written reports and presentations of those data
Strong critical, strategic, and analytical thinking skills
Experience in all aspects of protocol conduct, both early and late phase, including protocol writing, start-up, study execution, analysis and reporting
Experience in working closely with investigative sites, including principal investigators, sub-investigators, study coordinators and other site personnel involved in clinical trials
Skilled in clinical research and understand the process of pharmaceutical product development and approval
Able to function in a highly regulated environment and to adhere to all RayzeBio guidelines and standard operating procedures (SOP's)
Solid understanding of GCP and ICH guidelines
Preferred
Radiopharmaceutical experience is preferred but not required
Benefits
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
H1B Sponsorship
Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (213)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)
Funding
Current Stage
Public CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Recent News
2025-12-30
BioWorld Financial Watch
2025-12-29
2025-12-25
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