Senior Medical Director – Clinical Development, Prostate Cancer

🕒 August 7

🇺🇸 United States – Remote

💵 $306.8k - $371.8k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 29%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 strategy for prostate cancer assets • Own clinical development plans across the full lifecycle, from IND through Phase 3 registrational studies • Grow and manage the prostate cancer clinical team and recruit medical directors and clinical scientists as needed • Work with research and translational medicine teams on clinical-stage assets and pipeline molecules • Participate in business development and due diligence efforts • Engage BMS oncology leaders to develop combination strategies and support prostate disease-area strategies • Provide medical direction and scientific and clinical leadership for early- and late-development molecules • Support IND preparation and regulatory authority interactions • Design and execute Phase 1 through Phase 3 clinical trials and conduct medical monitoring • Lead cross-functional study teams covering study design, implementation, monitoring, analysis, and reporting • Interact with clinical investigators and thought leaders to design development plans • Partner with investigators and CROs to design and implement clinical studies • Contribute to protocols, investigator brochures, clinical study reports, and other clinical and regulatory documents • Conduct investigator meetings and lead site qualification and initiation visits • Execute drug-development strategies, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets • Translate research and nonclinical findings into clinical development opportunities • Oversee data review and Independent Data Monitoring Committees • Ensure clinical trials follow applicable pharmaceutical-industry ethical guidelines • Maintain relationships with clinical investigators and thought leaders • Lead regulatory interactions, prepare briefing documents, attend and present at health-authority meetings, and oversee regulatory submissions • Supervise and mentor clinical scientists and medical directors • Leverage AI to drive program, portfolio, or functional performance through prioritization and scaled adoption

🎯 Requirements

• MD or equivalent is required • At least 10 years of pharmaceutical/biotech/academic experience in oncology solid tumor clinical development • Drug development experience in prostate cancer is required • Sub-specialty training in oncology is ideal • Radiopharmaceutical experience is preferred but not required • Demonstrated leadership of clinical and cross-functional teams in a biotech environment • Experience managing multiple stakeholder engagements across development and commercial organizations • Experience in NDA/MAA preparation and submission and complex health authority interactions globally • Experience in all aspects of early- and late-phase 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 adhere to RayzeBio guidelines and SOPs • Solid understanding of GCP and ICH guidelines • Strong written, oral, and presentation skills • Strong critical, strategic, and analytical thinking skills • Willingness to travel approximately 30% of the time

🏖️ Benefits

• Additional discretionary incentive cash and stock opportunities • Wellbeing support • Retirement and financial protection benefits • Medical, dental, vision, life and disability insurance offerings • Flexible Time Off (FTO) for U.S.-based exempt employees • 11 paid company holidays each year • 160 hours of paid vacation annually for new hires for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico • 3 optional holidays for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico • Paid sick leave, depending on eligibility • Up to two paid volunteer days per year, depending on eligibility • Summer hours flexibility • Leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs • Annual Global Shutdown between Christmas Day and New Year's Day for eligible employees • Reasonable workplace accommodations/adjustments and ongoing support