Executive Director, Oncology Clinical Development
vor 2 Monaten
Bristol Myers Squibb is seeking a highly experienced and skilled Senior Executive Director to lead our Late Clinical Development Oncology team. As a key member of our R&D organization, you will be responsible for the development, clinical monitoring, interpretation, and analysis of all clinical trials and protocols in late-stage development, as well as all global regulatory submissions and procedures.
Key ResponsibilitiesDevelop and execute a strategic vision for the Late Clinical Development Oncology team, driving innovation and excellence in clinical research and development.
Lead a team of clinical development professionals, providing guidance, mentorship, and coaching to ensure the success of our clinical trials and programs.
Collaborate with cross-functional teams, including Early Clinical Development, Regulatory, and Commercial, to ensure seamless transition from Phase 1 to Phase 2 and beyond.
Develop and maintain relationships with key thought leaders and experts in oncology and immuno-oncology drug development, staying up-to-date on the latest scientific advancements and trends.
Manage all clinical components of regulatory documents, including filings for initial registration and life cycle management indications.
Represent BMS in critical discussions with health authorities, interpreting clinical data, clinical trial design, and safety and efficacy profiles of our compounds.
Develop and promote a workplace culture that values diversity of thought, promotes integrity, and creates an atmosphere that supports coaching and fosters accountability.
MD (Board certified in oncology preferred) with significant clinical research and drug development expertise and leadership experience (10 years or greater) in oncology.
Deep understanding of early-stage through late-stage drug development issues and challenges, as well as extensive experience designing and conducting innovative Phase 2 and Phase 3 clinical trials within related areas of focus.
Significant successful global drug filing expertise and regulatory interaction experience (i.e. NDA, ODAC, oral explanation, etc.).
Knowledge, experience, and successful professional relationships with external oncology thought leaders.
Successful experience building, leading, and motivating teams of clinical research professionals, including MDs, PhDs, and/or PharmDs.
Documented success navigating and delivering results within a highly matrixed work environment; effective cross-business unit and divisional collaboration a must (i.e., partnering across all aspects of research, development, and early commercial).
Global experience and ability to interface with clinical development leaders across Europe, Asia, Latin America, and US is required.
Knowledge or experience in immuno-oncology is desired.
Experience interacting with business development and licensing, particularly helping to evaluate the technical and franchise aspects for potential in-licensing opportunities that shape the oncology strategy is important.
Bristol Myers Squibb offers a competitive salary and benefits package, as well as opportunities for professional growth and development. We are committed to creating a diverse and inclusive work environment that values integrity, innovation, and collaboration.
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