Pfizer · 2 months ago
Vice President, Internal Medicine Regulatory Strategy
United States - Massachusetts - Cambridge
Full-time
Hybrid
Director/Executive
$280K/yr - $467K/yr
10+ years expPfizer is a leading biopharmaceutical company, and they are seeking a Vice President for Internal Medicine Regulatory Strategy. This role involves providing regulatory guidance and leadership for Pfizer’s Internal Medicine portfolio, ensuring compliance and facilitating timely approvals for products through innovative regulatory strategies.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
No H1B
Responsibilities
Provides regulatory expertise and leadership within the assigned portfolio, and other disease areas as relevant including ensuring global regulatory strategies for all projects and products within the assigned portfolio, as relevant are developed and implemented
Responsible for developing and maintaining an in-depth regulatory knowledge of the portfolio including current and emerging global guidelines and regulator’s latest thinking, relevant regulatory approaches and actions; and status of competitor products
Partners with leaders in R&D and Commercial teams to develop strong global regulatory strategies for projects and products
Engages in appropriate activities to influence the regulatory environment including developing strong working relationships with regulators, professional bodies, external experts and opinion leaders
Owns resource allocation for GRS IM
Champions flexible approaches to ensure efficient and effective resource utilization
May assume responsibility for other activities/functions within GRS as required
Ensures development of all staff functional line help them achieve their full potential
Qualification
Required
Advanced Scientific Degree (M.D., Ph.D., PharmD) with a minimum of 10 years' experience in drug, device, development and/or commercialization
Subject-matter expertise within assigned therapeutic area includes global regulatory strategy experience in the cardiovascular, renal and metabolic disease (CVRM) areas
Has significant experience and track record of achievements in the chronic weight management area and GLP-1 landscape, through prior regulatory experience, and direct product development
Proven track record of success in negotiating with global health authorities and in representing interests to external stakeholders
Demonstrated strategic thinking and ability to integrate strategies into actionable plans
Proven ability to function autonomously at a senior level in a highly matrixed organization
Proven track record of successful management of staff and complex regulatory, program management or business issues
Proven ability to lead with an innovative and agile mindset as well as creatively execute strategic plans
Preferred
20+ years demonstrable experience in drug and/or device development or relevant experience in the pharmaceutical industry, preferably in Drug Development or Clinical Research, ideally within Regulatory Affairs
Benefits
Participation in Pfizer’s Global Performance Plan with a bonus target of 30.0% of the base salary
Eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Company
Pfizer
Pfizer is a biopharmaceutical company that discovers, develops, and delivers medicines and vaccines.
10001+ employees
Funding
Current Stage
Public CompanyTotal Funding
$38BKey Investors
Starboard Value
2025-11-21Post Ipo Debt· $6B
2024-10-07Post Ipo Equity· $1B
2023-05-16Post Ipo Debt· $31B
Leadership Team
Albert Bourla
Chief Executive Officer
Ian Read
Chief Executive Officer
Recent News
2026-01-21
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2026-01-21
2026-01-20
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