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About the role
Key responsibilities & impact- Provide medical and scientific expertise for Clinical Trials and accountability for one or more clinical studies
- Design development strategy for multiple protocols
- Monitor study safety issues and provide input to serious adverse events (SAEs) reports
- Provides protocol specific training to study team, investigators, and others
- Conduct medical review and interpretation of efficacy and safety data from clinical trials
Requirements
What you’ll need- Medical degree (M.D./D.O. or equivalent)
- 4+ years’ work experience
- Licensed by a health authority to prescribe medicines for at least two years
- Ability to critically evaluate medical/scientific information
- Understanding of design, development, and execution of clinical programs and studies
- Documented experience in pharmaceutical industry related to clinical research programs and registration activities
- Experience managing multiple studies
Benefits
Comp & perks- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation
- Paid holiday
- Paid personal days
- Paid caregiver/parental leave
- Paid medical leave
- Health benefits including medical, prescription drug, dental, and vision coverage
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trialsprotocol designsafety monitoringmedical reviewdata interpretationadverse event reportingclinical researchstudy managementpharmaceutical developmentclinical program execution
Soft Skills
critical evaluationtrainingcommunicationteam collaborationaccountabilityproblem-solvingorganizational skillsleadershipattention to detailinterpersonal skills
Certifications
medical degree (M.D./D.O. or equivalent)licensed by health authority
