Senior Medical Director – Clinical Development, Prostate Cancer

This is a fully remote position, open to applicants in United States.

📋 Description

• Engage with clinical investigators and thought leaders to develop a clinical development plan for selected drug candidates.

• Lead internal study teams and collaborate with investigators and CROs to design and execute clinical studies.

• Work closely with GPLs to ensure the development and commercial optimization of Rayze Bio assets.

• Contribute to the preparation of protocols, investigator brochures, clinical study reports, and review various clinical trial and regulatory documents.

• Conduct investigator meetings and oversee site qualification and initiation visits with clinical trial investigators.

• Implement drug development strategic plans, create contingency plans, offer technical and strategic guidance, and achieve milestones and budgetary goals.

• Translate research and nonclinical study findings into clinical development opportunities.

• Supervise Data Review and Independent Data Monitoring Committees.

• Conduct clinical trials adhering to ethical guidelines relevant to the pharmaceutical industry, ensuring compliance with external regulations.

• Establish and nurture positive relationships with clinical trial investigators and thought leaders.

• Serve as the clinical lead for regulatory interactions when necessary, including preparing briefing documents and participating in health authority meetings. Oversee regulatory submissions for assets targeting prostate cancer indications.

• Lead cross-functional study teams and provide supervision and mentorship to clinical scientists and medical directors in executing prostate cancer programs.

• Recruit, build, and manage a team of medical directors and clinical scientists as necessary based on programmatic needs.

• Utilize AI to enhance program, portfolio, or functional performance through prioritization and widespread adoption.

• Willing to travel approximately 30% of the time.

⛳️ Requirements

• MD or equivalent, preferably with subspecialty training in oncology and a minimum of 10 years of experience in pharmaceutical/biotech/academic settings focused on oncology solid tumor clinical development (radiopharmaceutical experience is a plus but not mandatory).

• Experience in drug development specifically related to prostate cancer is essential.

🏝️ 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.

• Work-life benefits include: Paid Time Off for 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). For Phoenix, AZ, Puerto Rico, and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours of annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs, as well as an annual Global Shutdown between Christmas and New Year's Day. All global employees, both full-time and part-time, who are actively employed at and compensated directly by BMS at the end of the calendar year are eligible for the Global Shutdown.