Clinical Development Medical Director, Breast Oncology
$239,900–$399,800 year
HybridNew York City, New York, United States or Cambridge, Massachusetts, United States
Job Summary
Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring while leading sub teams in clinical development for the prifetrastat program. Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, and regulatory authorities, and lead the development and maintenance of clinical trial and regulatory documents. Collaborate with the Global Development Team to create and refine development strategies, interpret clinical data to identify key findings, and communicate implications to internal and external stakeholders. Lead peer-to-peer interactions with investigators and provide clinical development leadership across several study teams. Represent the company in external engagements or as a committee member in joint collaborations.
Required Qualifications
- Primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university
- 4+ years of experience in biopharmaceutical industry in clinical research and development
- Licensed by a licensing body/health authority to prescribe medicines independent of Supervision for at least 2 years post their intern/house officer/foundation period
- Authorization to be employed in the U.S.
- Permanent work authorization in the United States
Desired Qualifications
- Board certified/eligible in oncology or equivalent
- Breast Oncology experience (2+ years)
- Late phase clinical development experience
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