Represent Clinical on the Global Medicine Team and be accountable for clinical development for assigned asset(s)
Lead the cross-functional Clinical Development Team
Design, execution, and interpretation of studies in support of regulatory submissions
Create and gain endorsement for the Clinical Development Plan and associated protocol design documents
Provide specialized monitoring support if required and engage with external companies
Drive strategic insight generation to support clinical development strategy

Requirements

BS with 12 yrs or PhD with 7 yrs, relevant clinical/industry experience
Experience leading large cardiometabolic late-stage development programs
Relevant experience and track record of success in academia and/or the biopharmaceutical industry in clinical research and development
Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management
Demonstrated clinical/medical, administrative, and project management capabilities
Effective verbal and written communication skills

Benefits

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 including medical, prescription drug, dental, and vision coverage

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical developmentstudy designregulatory submissionsprotocol designmonitoring supportstrategic insight generationadverse event managementproject management

Soft Skills

leadershipcommunication