Global Safety Program Lead/Sr Medical Director
AstraZeneca · Boston, Massachusetts, United States of America · Global
Medical Affairs
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Not yet analysed
Demand90
Career growth85
Healthcare fit80
Remote potential60
5-year outlook
Senior Director roles in global pharma typically command high six-figure to seven-figure total compensation, with strong growth potential given the criticality of drug safety in regulatory approval and market success.
Clinical license
Required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-09-14
Intelligence details
Why this is worth applying to
This is an excellent opportunity for physicians with extensive clinical experience and a track record in pharmacovigilance or drug development. It offers significant strategic influence and leadership, but requires deep domain expertise and is not suitable for early-career clinicians.
Who should apply
Experienced physicians (MD/DO) with clinical practice background, ideally with prior roles in drug safety, pharmacovigilance, or clinical development in pharma or biotech. Also relevant for physicians with regulatory affairs or medical affairs experience.
CV angle
Emphasize clinical expertise, direct patient care experience, and any prior involvement in clinical trials, safety monitoring, or regulatory submissions. Highlight leadership in multidisciplinary teams and strategic decision-making. Frame clinical experience as foundational to understanding benefit-risk assessment and patient safety.
Skills to highlight
- Pharmacovigilance
- Risk Management Plans
- Regulatory Compliance
- Clinical Trial Design
- Safety Surveillance
- Strategic Leadership
- Cross-functional Collaboration
- Benefit-Risk Assessment
Role summary
A senior leadership role at AstraZeneca accountable for the global safety strategy and oversight of assigned drug assets, leading a team of safety physicians and scientists, and ensuring compliance with regulatory standards.
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