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.
Benefits
401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation
Holiday and personal days
Paid caregiver/parental and medical leave
Health benefits including medical, prescription drug, dental and vision coverage
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 filingssafety data evaluationpharmacology data evaluationefficacy data evaluationliterature reviewmanuscript developmentpresentation development