Clinician serving within a Pfizer vaccine development program, leading clinical studies with safety oversight and regulatory support. Responsible for medical expertise and collaboration with various teams on clinical trials.
Responsibilities
Serve as a Clinician within a Pfizer vaccine development program
Clinical lead for one or more studies within a clinical program
Provide medical and scientific expertise and oversight for Clinical Trials
Accountable for safety across the study
Provide study team with medical advice for all medical issues during risk assessment and mitigation planning
Ensure development of and adherence to the Safety Surveillance Review Plan (SSRP)
Monitor study safety issues and provide input to serious adverse events (SAEs) reports
Participate in the Safety Review Team to evaluate medical benefits/risks
Provide appropriate medical context for risk factors, medical history
Contribute towards the medical input during protocol development and updates to the clinical development plan
Provide clinical input to protocol/study team for monitoring guidelines, statistics analysis plans, etc.
Collaborate with regulatory authorities, key opinion leaders, and principal investigators
Requirements
Medical degree (M.D./D.O. or equivalent)
Licensed by a health authority to prescribe medicines (independent of supervision) for at least one year (post "intern/houseman" year)
0-4 years' work experience
Possesses the ability to critically evaluate medical/scientific information
Excellent written and oral communication
Understands the design, development, and execution of clinical programs and studies
Capacity to adapt to a fast pace and changing environment
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 to include medical, prescription drug, dental and vision coverage
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