Associate Director, Clinician – Vaccines, MD
Pfizer
full-time
Posted on:
Location Type: Office
Location: Pearl River • New York, Pennsylvania • 🇺🇸 United States
Visit company websiteSalary
💰 $182,000 - $303,300 per year
Job Level
Senior
About the role
- Serve as a Clinician within a Pfizer vaccine development program and may serve as clinical lead for one or more studies
- Provide medical and scientific expertise and oversight for Clinical Trials; single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies
- Accountable for safety across the study and ensure development of and adherence to the Safety Surveillance Review Plan (SSRP)
- Perform and document regular review of individual subject safety data and review of cumulative safety data with the safety risk lead
- Monitor study safety issues and provide input to serious adverse events (SAEs) reports and provide medical context for AEs/SAEs
- Participate in Safety Review Team, review literature to respond to safety questions and communicate safety information to sites
- Contribute medical input during protocol development, clinical development plan updates, and country feasibility
- Provide clinical input to protocol/study team for monitoring guidelines, statistical analysis plans, ICDs, clinical review forms, data edit checks, and data quality planning
- Contribute to CRO/vendor selection and ensure medical/technical requirements for data integrity
- Contribute to medical review and interpretation of efficacy and safety data; collaborate on top-line reports and clinical study reports
- Provide protocol specific training to study team, investigators, CRAs and interact with DMCs and steering committees
- Support study team with study closeout, audit responses, inspection readiness, and interact with regulatory authorities and KOLs
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)
- Has utilized the license to prescribe medicines in a patient care setting for an aggregate duration of at least one 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
- Position requires permanent work authorization in the United States
- Preferred: Documented work experience/knowledge of statistics
- Preferred: Training and experience in infectious diseases and/or infection control in the hospital setting
- Preferred: Experience with investigational clinical trials
- No pharmaceutical industry experience required
Benefits
- Eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 22.5% of the base salary
- Eligibility to participate in Pfizer’s share based long term incentive program
- 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
- Relocation assistance may be available based on business needs and/or eligibility
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trialssafety surveillance review planmedical reviewstatistical analysisdata integrityprotocol developmentsafety data monitoringadverse events reportingclinical study reportsinfectious diseases
Soft skills
critical evaluationwritten communicationoral communicationadaptabilitycollaborationoversightaccountabilitytraininginterpersonal skillsproblem-solving
Certifications
medical degree (M.D./D.O. or equivalent)licensed to prescribe medicines