Clinical Development Leadership on Study Teams and Development Subteams
Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring
Lead peer-to-peer interactions with investigator
Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities
Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross-functional team
Oversees and provides clinical development leadership across several study teams
Serves as the Clinical Development Lead on subteams including for Marketing Authorization Applications
Collaborates with the Global Development Team to create and refine development strategies
Represents the company in external engagements or as committee members in joint collaborations
Collaborate with Clinical Scientist to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders
Maintains a high level of clinical expertise and professional competence by staying abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans
Requirements
Medical degree with 5+ years clinical/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
medical monitoringdata reviewsafety monitoringclinical trial documentationregulatory documentationclinical data interpretationdevelopment strategies