Senior Medical Director – Clinical Development, Prostate Cancer

🕒 August 7

🇺🇸 United States – Remote

💵 $306.8k - $371.8k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

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Bristol Myers Squibb

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1887

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Bristol Myers Squibb is a global biopharmaceutical company that is dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. Their areas of focus include cardiovascular health, cell therapy, immunology, and oncology. With a commitment to transforming patient outcomes through pioneering science, Bristol Myers Squibb partners with a worldwide network of researchers, healthcare providers, and other stakeholders. They aim to lead in innovation for patients while fostering diversity and inclusion within their workforce.

📋 Description

• Develop and execute clinical development strategies and plans for prostate cancer assets from IND through Phase 3 registrational studies • Grow and manage the prostate cancer clinical team as needed for additional programs • Collaborate with research and translational medicine teams on clinical-stage assets and pipeline molecules • Participate in business development and due diligence efforts to expand RayzeBio’s portfolio • Engage BMS oncology leaders on combination strategies and prostate disease-area strategies • Provide medical direction and scientific and clinical expertise for early- and late-development molecules • Support IND preparation and regulatory authority interactions • Design, execute, monitor, analyze, and report Phase 1 to Phase 3 clinical trials • Lead cross-functional study teams and ensure programs meet patient and business needs • Interact with clinical investigators and thought leaders to develop plans for drug candidates • Partner with investigators and CROs to design and implement clinical studies • Contribute to protocols, investigator brochures, clinical study reports, and regulatory documents • Conduct investigator meetings and lead site qualification and initiation visits • Execute strategic drug development plans, develop contingency plans, advise on technical and strategic matters, and meet milestones and budgets • Translate research and nonclinical findings into clinical development opportunities • Oversee Data Review and Independent Data Monitoring Committees • Ensure ethical conduct of clinical trials and compliance with pharmaceutical industry guidelines • Establish relationships with investigators and thought leaders • Lead regulatory interactions and oversee regulatory submissions for prostate cancer indications • Supervise and mentor clinical scientists and medical directors • Recruit, build, and manage medical director and clinical scientist teams as needed • Leverage AI to drive program, portfolio, or functional performance

🎯 Requirements

• MD or equivalent is required • Sub-specialty training in oncology is ideal • At least 10 years of pharmaceutical, biotech, or academic experience in oncology solid tumor clinical development • Drug development experience in prostate cancer is required • Radiopharmaceutical experience is preferred but not required • Demonstrated leadership of clinical and cross-functional teams in a biotech environment • Demonstrated ability to manage multiple stakeholder engagements across development and commercial organizations • Strong written and oral communication skills, including presentation skills • Strong critical, strategic, and analytical thinking skills • Experience in NDA/MAA preparation and submission and complex global health authority interactions • Experience across protocol conduct, including protocol writing, study start-up, execution, analysis, and reporting • Experience working with investigative sites, principal investigators, sub-investigators, study coordinators, and other clinical trial personnel • Skilled in clinical research and pharmaceutical product development and approval processes • Ability to function in a highly regulated environment and follow RayzeBio guidelines and SOPs • Solid understanding of GCP and ICH guidelines • Willingness to travel approximately 30% of the time

🏖️ Benefits

• Additional incentive cash and stock opportunities (based on eligibility) • Medical, pharmacy, dental, and vision care • BMS Well-Being Account • BMS Living Life Better • Employee Assistance Programs (EAP) • 401(k) plan • Short- and long-term disability insurance • Life insurance • Accident insurance • Supplemental health insurance • Business travel protection • Personal liability protection • Identity theft benefit • Legal support • Survivor support • Flexible time off for US exempt employees, with manager approval • 11 paid national holidays • 160 hours annual paid vacation for eligible Phoenix, AZ, Puerto Rico and RayzeBio employees • 3 optional holidays for eligible Phoenix, AZ, Puerto Rico and RayzeBio employees • Unlimited paid sick time, based on eligibility • Up to 2 paid volunteer days per year, based on eligibility • Summer hours flexibility, based on eligibility • Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs • Annual Global Shutdown between Christmas and New Years Day