Clinical Development Medical Director, Breast Oncology

Clinical Development Medical Director (prifetrastat program)

Responsibilities

• Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring.
• Lead peer-to-peer interactions with investigators.
• Serve as point of contact for clinical issues among study teams, investigators, ethics committees, steering committees, and regulatory authorities.
• Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional teams.
• Provide clinical development leadership across several study teams.
• Represent Clinical Development on subteams including for Marketing Authorization Applications.
• Collaborate with Global Development to create/refine development strategies.
• Represent the company in external engagements/joint collaborations.
• Collaborate with Clinical Scientists to review/interpret clinical data, identify key findings, and communicate to stakeholders.
• Stay current with literature and guidelines to advise and drive current/future clinical development plans.

Basic Qualifications

• Primary medical degree (MD, DO, MBBS, MBChB) from a recognized school.
• 4+ years biopharmaceutical clinical research & development experience.
• Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation.

Preferred Qualifications

• Board certified/eligible in oncology (or equivalent).
• Breast oncology experience (2+ years).
• Late phase clinical development experience.

Travel/Location & Benefits

• Hybrid: live within commuting distance; work onsite ~2.5 days/week.
• Travel to scientific conferences/meetings several times per year.
• Relocation support may be available.
• Eligible for Global Performance Plan bonus (25% target) and share-based long-term incentive; comprehensive benefits including 401(k), paid time off, caregiver/parental and medical leave, and medical/dental/vision.