Clinical Development Medical Director, Oncology
Pfizer
9 hours ago
Remote friendly (La Jolla, CA)
United States
Clinical Research and Development
Job Responsibilities
- Collaborate with Clinical Scientist(s) to provide clinical leadership across 2-3 study team(s) that is scientifically rigorous and aligns with company objectives.
- Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development and maintenance of clinical trial and regulatory documents with Clinical Scientist and the cross-functional team.
- Collaborate with Clinical Scientist to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders.
- Stay abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans.
Basic Qualifications
- Medical degree (Required)
- Clinical Development experience (Required)
- 2–5 years industry experience (Required)
Preferred Qualifications
- Late-stage clinical development experience (Preferred)
- Thoracic experience (Preferred)
- Board certified/eligible in oncology or equivalent (Preferred)
Work Location / Travel
- Hybrid role; live within commuting distance and work on-site an average of 2.5 days per week
- Travel to conferences and team meetings ~4 times per year
Benefits (as stated)
- Base salary range: $239,900.00–$399,800.00
- Bonus target: 25% of base salary; eligibility for share-based long-term incentive
- Comprehensive benefits including 401(k) with matching contributions, paid vacation/holidays/personal days, paid caregiver/parental and medical leave, and medical/prescription drug/dental/vision coverage
- Collaborate with Clinical Scientist(s) to provide clinical leadership across 2-3 study team(s) that is scientifically rigorous and aligns with company objectives.
- Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development and maintenance of clinical trial and regulatory documents with Clinical Scientist and the cross-functional team.
- Collaborate with Clinical Scientist to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders.
- Stay abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans.
Basic Qualifications
- Medical degree (Required)
- Clinical Development experience (Required)
- 2–5 years industry experience (Required)
Preferred Qualifications
- Late-stage clinical development experience (Preferred)
- Thoracic experience (Preferred)
- Board certified/eligible in oncology or equivalent (Preferred)
Work Location / Travel
- Hybrid role; live within commuting distance and work on-site an average of 2.5 days per week
- Travel to conferences and team meetings ~4 times per year
Benefits (as stated)
- Base salary range: $239,900.00–$399,800.00
- Bonus target: 25% of base salary; eligibility for share-based long-term incentive
- Comprehensive benefits including 401(k) with matching contributions, paid vacation/holidays/personal days, paid caregiver/parental and medical leave, and medical/prescription drug/dental/vision coverage