Senior Late-Stage Oncology Clinical Development Scientist

Pfizer Inc; New York (NY); Hybrid; USD 177,000 - 294,000; Full time

Benefits offered by this job

401(k) with Pfizer Matching Contribu­t

Pfizer Retirement Savings Contribution

Paid vacation, holidays and personal

Health benefits: medical, dental, viz

Job summary

Pfizer Inc. is seeking a senior clinical development expert to oversee scientific integrity, data quality, and regulatory readiness for late-stage oncology programs. You will lead cross-functional collaboration, author essential trial documents, and drive data review strategies across pivotal trials.

Candidates should have deep clinical research experience, oncology expertise, and a proven track record in regulatory submissions and inspections within industry/CRO settings. Hybrid on-site role.

Qualifications

• PhD/Pharm D or MS/BA with extensive Clinical Research experience in industry/CRO.
• Experience in phase 3/pivotal Oncology trials, regulatory submissions and inspections.
• Strong knowledge of ICH, GCP and global regulatory requirements.

Responsibilities

• Provide scientific oversight, data integrity and quality for clinical trials in oncology programs.
• Partner with cross-functional teams to execute trials and implement development strategies.
• Represent the study team in governance meetings and support regulatory submissions.
• Author study documents and contribute to clinical study reports and regulatory responses.
• Set data review strategy and lead quality data collection and trend analysis.
• Monitor emerging safety data and keep medical/clinical teams informed of changes.
• Ensure compliance with SOPs, regulations and quality standards; drive process improvements.

Skills

Clinical Research

ICH guidelines

GCP

Regulatory knowledge

Data interpretation

Scientific communication

Education

PhD/Pharm D in a relevant Science discipline

MS in a relevant Science discipline

BA/BS in a relevant Science discipline

Tools

Microsoft Office

Job description

Pfizer Inc. is seeking a senior clinical development expert to oversee scientific integrity, data quality, and regulatory readiness for late-stage oncology programs. You will lead cross-functional collaboration, author essential trial documents, and drive data review strategies across pivotal trials.

Candidates should have deep clinical research experience, oncology expertise, and a proven track record in regulatory submissions and inspections within industry/CRO settings. Hybrid on-site role.