Senior Manager, Late-Stage Oncology Clinical Development

Pfizer; New York (NY); Hybrid; USD 139,000 - 232,000; Full time

Benefits offered by this job

Health benefits

401(k) with Pfizer matching

Bonus program

Job summary

Pfizer is seeking an Oncology Late Stage Clinical Development Scientist, Senior Manager (Non MD) to provide scientific oversight, data integrity, and quality control for late-stage oncology trials. The role partners with Clinical Operations, Safety, Biostatistics, Regulatory and Study Teams to drive strategy and execution in a global program.

You will author study documents, lead data reviews, oversee safety assessments, and represent the study in governance meetings.

Qualifications

• PhD/PharmD with 2+ years pharma/industry CRO experience or MS with 5+ years OR BA/BS with 7+ years in a similar role.
• Experience in oncology clinical trial development and Phase 3/pivotal studies.
• Knowledge of ICH, GCP, FDA/EMA regulations and global regulatory expectations.

Responsibilities

• Provide scientific oversight and data integrity for late-stage oncology trials.
• Partner with Clinical Operations, Safety, Biostatistics, Regulatory to drive study strategy and execution.
• Author protocols, ICFs, and contribute to CSRs and regulatory responses.
• Lead data reviews, discuss emerging trends with governance bodies.
• Ensure SOP compliance and drive quality improvements.

Skills

Oncology knowledge

Clinical data review

Cross-functional collaboration

Regulatory submissions

Communication

Education

PhD/PharmD in a relevant Science

MS in a relevant Science

BA/BS in a relevant Science

Tools

Microsoft Office

Clinical software

Job description

Pfizer is seeking an Oncology Late Stage Clinical Development Scientist, Senior Manager (Non MD) to provide scientific oversight, data integrity, and quality control for late-stage oncology trials. The role partners with Clinical Operations, Safety, Biostatistics, Regulatory and Study Teams to drive strategy and execution in a global program.

You will author study documents, lead data reviews, oversee safety assessments, and represent the study in governance meetings.