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About the role
- Clinical Development Scientist providing scientific oversight and quality support for clinical trials in Pfizer's Internal Medicine portfolio. Involved in protocol development, safety oversight, and regulatory document authoring.
Responsibilities
- Provides support of scientific oversight, data integrity, and quality of clinical trials
- Contributes to the development of efficient protocols and supports clinical colleagues
- Reviews, reports, and manages protocol deviations and safety data
- Reviews and approves country and site selection criteria
- Authoring clinical sections of regulatory documents and clinical study reports
Requirements
- BA/BS with 4+ years of experience OR MA or MS with 2+ years of experience OR PhD with 0+ years of experience
- Demonstrated clinical, administrative, and project management capabilities
- Excellent verbal and written communication skills in English
- Proven analytical skills with the ability to work on large data sets
- Effective communication, presentation, and organizational skills
- Demonstrated scientific writing skills in English
- Must have flexibility to adapt and navigate through an ever-changing work environment
- Must have relevant personality features and competencies supporting the responsibilities
Benefits
- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation
- Paid holiday and personal days
- Paid caregiver/parental and medical leave
- Health benefits including medical, prescription drug, dental and vision coverage
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