Salary
💰 $226,300 - $377,100 per year
About the role
- Lead clinical study teams and ensure appropriate medical monitoring for ongoing clinical studies.
- Lead development and maintenance of clinical documents (e.g. protocols and amendments, investigator brochures, clinical study reports).
- Lead development of clinical study documents to be used in regulatory interactions and filings.
- Develop manuscripts, abstracts and presentations for scientific meetings.
- Evaluate safety, pharmacology, and efficacy data from ongoing and completed studies to inform clinical strategy.
- Conduct literature reviews and prepare summaries to support clinical development strategies.
- Support ongoing study activities and collaborate across functions for study level deliverables.
Requirements
- Medical degree.
- 2-5 years industry experience.
- Board certified/eligible in oncology or equivalent preferred.
- Health benefits to include medical, prescription drug, dental and vision coverage.
- 401(k) plan with Pfizer Matching Contributions.
- Additional Pfizer Retirement Savings Contribution.
- Paid vacation, holiday and personal days.
- Paid caregiver/parental and medical leave.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical study designmedical monitoringclinical document developmentregulatory interactionssafety evaluationpharmacology analysisefficacy data evaluationliterature reviewmanuscript developmentpresentation preparation
Soft skills
leadershipcollaborationcommunicationorganizational skillsstrategic thinking
Certifications
medical degreeboard certified in oncology