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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and implementing global regulatory strategies for Obesity and Chronic Weight Management, ensuring compliance with regulatory standards while effectively collaborating with cross-functional teams and Health Authority contacts.
Highest-signal resume keywords
Global Regulatory Strategy DevelopmentRegulatory Submissions ManagementCross-Functional CollaborationHealth Authority Relationship ManagementRisk Mitigation and Communication
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Regulatory StrategyRegulatory ComplianceLabeling ActivitiesRisk Register ManagementRegulatory Query Responses
Soft Skills
Influencing PeersCollaborating with TeamsCoaching and Developing Others
Industry Keywords
Obesity ManagementChronic Weight ManagementGlobal Regulatory EnvironmentHealth Authority ContactsProject Management
About the role
Key responsibilities & impact- Develop and implement global regulatory strategy for Pfizer's Obesity and Chronic Weight Management portfolio
- Act as global regulatory strategist and provide expertise to the Global Regulatory Strategic Team and cross-functional forums
- Lead global regulatory strategies and implementation plans, including core labels and risk registers
- Integrate input from regional and in-country regulatory colleagues
- Ensure regulatory contributions meet strategy objectives, standards, timelines, and probability-of-success goals
- Partner with project, commercial, and other customer groups to meet business needs
- Manage global submissions and ensure complete, timely, fit-for-purpose packages across key markets
- Monitor regulatory plans, communicate progress and variances to the Global Regulatory Lead and senior management, and mitigate risks
- Establish and communicate aligned global regulatory positions on key issues across regions
- Influence the global regulatory environment through colleagues, Health Authority contacts, and trade associations
- Ensure business compliance with Regulatory standards
- Develop and maintain relationships with Health Authority contacts across global markets
- Coordinate submissions, regulatory-query responses, labeling activities, and other assigned regulatory tasks
- Report to the Obesity Global Regulatory Portfolio Lead and collaborate with clinical, project management, development operations, safety, manufacturing, legal, medical, commercial, and external regulatory stakeholders
Requirements
What you’ll need- Bachelor's degree with at least 8+ years of experience
- Master's degree with at least 7+ years of experience is nice to have
- PhD with 5+ years of experience is nice to have
- MD with 4+ years of experience is nice to have
- Experience outside regulatory strategy, particularly medical affairs, is positively weighted
- Breadth of diverse leadership experiences and capabilities, including influencing and collaborating with peers, developing and coaching others, and overseeing and guiding colleagues' work
- Candidates must be authorized to be employed in the U.S. by any employer
- Permanent work authorization in the United States is required
- U.S. work visa sponsorship is not available now or in the future
Benefits
Comp & perks- Flexible work arrangement with approximately 2.5 days per week in office under Log In For Your Day (LIFYD) requirements
- Relocation assistance may be available based on business needs and/or eligibility
- Professional growth opportunity through a 12-month secondment