Global Clinical Development Lead – Internal Medicine

Pfizer; San Diego (CA); Hybrid; USD 215,000 - 358,000; Full time

Job summary

Pfizer seeks a Global Development Lead to represent Clinical on the Global Medicine Team, accountable for clinical development for assigned assets in Internal Medicine. Leads cross-functional teams across clinical, pharmacology, statistics, safety, commercial, and operations for worldwide regulatory submissions.

The GDL creates the Clinical Development Plan and works as a key partner to internal teams and external collaborators, ensuring trial design, execution, and reporting align with

Qualifications

• BS with 12 yrs or PhD with 7 yrs, relevant clinical/industry experience.
• Experience leading cardiometabolic late-stage development programs.
• Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management.
• Demonstrated clinical/medical, administrative and project management capabilities.

Responsibilities

• Lead cross-functional Clinical Development Team across design, execution, interpretation of studies.
• Create and endorse Clinical Development Plan and protocol design documents.
• Lead regulatory submissions and contribute to submission deliverables (SCE, SCS, CDAs).
• Provide input for target product profiles and regulatory activities.
• Support external partnerships and internal lifecycle management.

Skills

Cross-functional leadership

Clinical development

Regulatory submissions

Project management

Medical/Scientific credibility

Leadership

Communication skills

Education

BS with 12 yrs experience

PhD with 7 yrs experience

Job description

Pfizer seeks a Global Development Lead to represent Clinical on the Global Medicine Team, accountable for clinical development for assigned assets in Internal Medicine. Leads cross-functional teams across clinical, pharmacology, statistics, safety, commercial, and operations for worldwide regulatory submissions.

The GDL creates the Clinical Development Plan and works as a key partner to internal teams and external collaborators, ensuring trial design, execution, and reporting align with