Global Oncology Clinical Physician Director

Bristol Myers Squibb; Cambridge (MA); Híbrido; USD 351.000 - 425.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive compensation

Comprehensive benefits

Flexible work models

Descripción de la vacante

Bristol Myers Squibb is seeking a Senior Director, Global Clinical Physician to lead medical accountability for oncology trials, guiding development from early phases to registrational execution. You will shape strategy, contribute to regulatory filings, and collaborate across Research, Early and Late Development to optimize outcomes.

The role requires MD-level expertise with 5+ years in clinical trial and drug development, and a track record of cross-functional leadership in oncology.

Formación

• MD with extensive clinical trial and drug development experience (5+ years)
• Strong leadership across cross-functional teams (Medical, Clinical, Regulatory)
• Deep oncology disease & translational biology knowledge
• Experience with regulatory submissions and clinical sections in multi-market submissions
• Ability to design strategic clinical development plans and protocols

Responsabilidades

• Medical accountability and oversight for oncology trials from Phase I to registrational execution
• Provide strategic insights into development plans and disease strategy
• Lead medical data review, safety assessments, and regulatory filings components
• Mentor and train study teams; collaborate with Clinical Scientists and CSOs
• Interact with Health Authorities and contribute to publications and submissions

Conocimientos

MD degree

Clinical development leadership

Oncology expertise

Regulatory strategy

Cross-functional leadership

Trial design & statistics

Strategic planning

Educación

MD (Medical Doctor)

Descripción del empleo

Bristol Myers Squibb is seeking a Senior Director, Global Clinical Physician to lead medical accountability for oncology trials, guiding development from early phases to registrational execution. You will shape strategy, contribute to regulatory filings, and collaborate across Research, Early and Late Development to optimize outcomes.

The role requires MD-level expertise with 5+ years in clinical trial and drug development, and a track record of cross-functional leadership in oncology.