Clinical Development Medical Executive Director (Prostate Cancer)
Pfizer, S.A. de C.V, San Diego, CA, United States
Clinical Development Medical Executive Director (Prostate Cancer)
United States - Massachusetts - Cambridge
United States - Washington – Bothell
United States - Pennsylvania - Collegeville
United States - New York - New York City
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
Pfizer Research & Development is the heart of Pfizer’s product pipeline, driving life‑changing medicines to the world.
This position is a Clinical Development Medical Executive Director supporting Prostate Cancer. The role is responsible for defining and executing the development strategy of oncology programs, leading one or more sub‑teams in clinical development, and serving as the clinical lead across multiple trials.
What You Will Achieve
Lead product‑specific Global Development Team.
Serve as subject‑matter expert on clinical issues.
Collaborate across cross‑functional teams to lead, develop, and execute clinical plans in alignment with Lifecycle Management and Integrated Product Plans.
Endorse clinical decisions before senior management reviews and governance bodies.
Oversee medical directors and Clinical Development Lead responsibilities.
Accountable for clinical strategy, trial design, execution, and delivery of results.
Integrate regulatory, statistical, and stakeholder input into study designs.
Act as primary interface with Development Review Committees.
Manage protocols, amendments, investigator brochures, and study reports.
Evaluate, interpret, report, and present study data.
Maintain clinical safety, pharmacology, and regulatory interactions.
Participate in evaluating business development opportunities.
Conduct medical monitoring activities including eligibility assessment and safety monitoring.
Lead peer‑to‑peer interactions with investigators.
Serve as point of contact for clinical issues with study team, investigators, ethics committees, steering committees, and regulatory authorities.
Support development and maintenance of clinical documents collaboratively with Clinical Scientists and the cross‑functional team.
Provide leadership across several study teams.
Represent the company in external engagements or as committee members.
Strategic Guidance & Clinical Insights
Lead the strategic development of therapies for one or more medicines in the designated therapeutic area.
Collaborate with the Global Development Product Lead as needed.
Review, interpret, and communicate clinical data, key findings, and implications internally and externally.
Maintain high‑level clinical expertise and professional competence.
Qualifications
Medical degree or advanced degree with relevant clinical/industry experience (generally 5+ years).
7+ years industry experience.
5+ years of experience leading diverse teams.
Prior management responsibilities of medical directors or clinical scientists.
Late‑phase drug development experience.
Board certified or eligible in oncology or equivalent (preferred).
Experience across multiple phases of clinical development and drug classes in oncology.
Experience leading NDA, BLA or MAA submissions (preferred).
Work Location Assignment
This hybrid role requires living within commuting distance, with onsite work average 2.5 days per week.
Annual base salary: $295,900.00 – $493,100.00, with bonus target 30% of base and eligibility for long‑term incentive program.
Benefits include 401(k) with Pfizer matching, additional retirement contributions, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and comprehensive health benefits.
Relocation support may be available on a case‑by‑case basis.
Citizenship: Candidates must be authorized to work in the U.S. (E‑Verify employer). U.S. work visa sponsorship is not available.
Pfizer is an E‑Verify employer. This position requires permanent work authorization in the United States.
Pfizer is committed to equal opportunity in employment regardless of race, color, religion, sex, sexual orientation, age, gender identity, national origin, disability or veteran status.
#J-18808-Ljbffr
United States - Massachusetts - Cambridge
United States - Washington – Bothell
United States - Pennsylvania - Collegeville
United States - New York - New York City
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
Pfizer Research & Development is the heart of Pfizer’s product pipeline, driving life‑changing medicines to the world.
This position is a Clinical Development Medical Executive Director supporting Prostate Cancer. The role is responsible for defining and executing the development strategy of oncology programs, leading one or more sub‑teams in clinical development, and serving as the clinical lead across multiple trials.
What You Will Achieve
Lead product‑specific Global Development Team.
Serve as subject‑matter expert on clinical issues.
Collaborate across cross‑functional teams to lead, develop, and execute clinical plans in alignment with Lifecycle Management and Integrated Product Plans.
Endorse clinical decisions before senior management reviews and governance bodies.
Oversee medical directors and Clinical Development Lead responsibilities.
Accountable for clinical strategy, trial design, execution, and delivery of results.
Integrate regulatory, statistical, and stakeholder input into study designs.
Act as primary interface with Development Review Committees.
Manage protocols, amendments, investigator brochures, and study reports.
Evaluate, interpret, report, and present study data.
Maintain clinical safety, pharmacology, and regulatory interactions.
Participate in evaluating business development opportunities.
Conduct medical monitoring activities including eligibility assessment and safety monitoring.
Lead peer‑to‑peer interactions with investigators.
Serve as point of contact for clinical issues with study team, investigators, ethics committees, steering committees, and regulatory authorities.
Support development and maintenance of clinical documents collaboratively with Clinical Scientists and the cross‑functional team.
Provide leadership across several study teams.
Represent the company in external engagements or as committee members.
Strategic Guidance & Clinical Insights
Lead the strategic development of therapies for one or more medicines in the designated therapeutic area.
Collaborate with the Global Development Product Lead as needed.
Review, interpret, and communicate clinical data, key findings, and implications internally and externally.
Maintain high‑level clinical expertise and professional competence.
Qualifications
Medical degree or advanced degree with relevant clinical/industry experience (generally 5+ years).
7+ years industry experience.
5+ years of experience leading diverse teams.
Prior management responsibilities of medical directors or clinical scientists.
Late‑phase drug development experience.
Board certified or eligible in oncology or equivalent (preferred).
Experience across multiple phases of clinical development and drug classes in oncology.
Experience leading NDA, BLA or MAA submissions (preferred).
Work Location Assignment
This hybrid role requires living within commuting distance, with onsite work average 2.5 days per week.
Annual base salary: $295,900.00 – $493,100.00, with bonus target 30% of base and eligibility for long‑term incentive program.
Benefits include 401(k) with Pfizer matching, additional retirement contributions, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and comprehensive health benefits.
Relocation support may be available on a case‑by‑case basis.
Citizenship: Candidates must be authorized to work in the U.S. (E‑Verify employer). U.S. work visa sponsorship is not available.
Pfizer is an E‑Verify employer. This position requires permanent work authorization in the United States.
Pfizer is committed to equal opportunity in employment regardless of race, color, religion, sex, sexual orientation, age, gender identity, national origin, disability or veteran status.
#J-18808-Ljbffr