Senior Manager, Late-Stage Oncology Clinical Development

Pfizer; San Diego (CA); Hybrid; USD 139,000 - 232,000; Full time

Job summary

Pfizer in the United States is seeking a leader to oversee science and data integrity for late-stage oncology programs, guiding development strategies and ensuring high-quality trial conduct.

You will collaborate with medical, clinical operations, and regulatory teams to drive protocol authoring, data review, safety assessment, and strategy alignment, while maintaining compliance with ICH, GCP, and global regulations.

Qualifications

• PhD/PharmD with 2+ years Clinical Research experience in industry/CRO
• Experience in oncology and phase 3 trials
• Excellent knowledge of ICH guidelines, GCP and global regulations
• Ability to work cross-functionally and present data to stakeholders

Responsibilities

• Lead scientific oversight and data integrity for assigned trials
• Partner with cross-functional teams to execute trials within programs
• Prepare study documents and support regulatory activities and submissions
• Define data review strategies and present findings to governance bodies
• Monitor safety signals and ensure SOP/regulatory compliance

Skills

Clinical research

Oncology knowledge

Data integrity

Regulatory submissions

SOP compliance

Education

PhD/PharmD in a relevant Science

MS in a relevant Science

BA/BS in a relevant Science

Tools

Microsoft Office

Clinical data systems

Job description

Pfizer in the United States is seeking a leader to oversee science and data integrity for late-stage oncology programs, guiding development strategies and ensuring high-quality trial conduct.

You will collaborate with medical, clinical operations, and regulatory teams to drive protocol authoring, data review, safety assessment, and strategy alignment, while maintaining compliance with ICH, GCP, and global regulations.