Senior Oncology Late-Stage Clinical Development Scientist

Pfizer Inc.; Groton (CT); Hybrid; USD 177,000 - 294,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

Pfizer Inc. in the United States seeks a trusted scientific leader to oversee late-stage oncology clinical trials, ensuring data integrity and quality across studies.

You will partner with cross-functional teams, drive governance discussions and contribute to regulatory documents. You will also shape data review strategies, monitor safety signals, and support Health Authority interactions while adhering to SOPs and global regulations.

Qualifications

• PhD/PharmD with 5+ years CR experience in industry/CRO
• MS with 7+ years CR experience in industry/CRO
• BA/BS with 10+ years CR experience in industry/CRO
• Oncology phase 3/pivotal space experience; sponsor-side preferred
• Solid tumor or hematology trial experience
• Experience leading a team
• Strong knowledge of clinical procedures, ICH, GCP, FDA/EMA
• Experience with large data sets
• Proficiency with Microsoft Office and relevant scientific software
• Excellent communication, presentation and organizational skills

Responsibilities

• Clinical development expert for assigned studies and knowledge in disease areas.
• Partner with clinical, medical, operations and other lines for trial success.
• Provide scientific oversight, data integrity and trial quality.
• Represent study team in governance meetings; support strategy.
• Author protocols, ICFs, and contribute to IBs, CSRs and regulatory documents.
• Set data review strategy; lead quality data collection and trend reviews.
• Analyze emerging safety and keep teams informed of changes.
• Follow SOPs and regulations; contribute to process improvements.

Skills

Clinical research

Team leadership

Regulatory submissions

Data integrity

ICH/GCP compliance

Education

PhD/PharmD

MS in science

BA/BS in science

Tools

Microsoft Office

Job description

Pfizer Inc. in the United States seeks a trusted scientific leader to oversee late-stage oncology clinical trials, ensuring data integrity and quality across studies.

You will partner with cross-functional teams, drive governance discussions and contribute to regulatory documents. You will also shape data review strategies, monitor safety signals, and support Health Authority interactions while adhering to SOPs and global regulations.