Associate Director, Clinical Development - Vaccine Lead

Pfizer

Pearl River (NY)

Hybrid

USD 189,000 - 315,000

Full time

4 days ago
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Benefits offered by this job

Hybrid work 2.5 days on-site
Competitive benefits

Job summary

Pfizer seeks a Clinician within a vaccine development program in the United States. This role may serve as clinical lead for one or more studies, working closely with the global clinical program lead to ensure execution and accountability for design, monitoring, and reporting.

The clinician provides medical oversight for Clinical Trials, supports regulatory interactions, and ensures patient safety through risk assessment, safety reviews, and data interpretation across trial sites.

Qualifications

  • Medical degree and licensure to practice.
  • 0-4 years' work experience.
  • Ability to critically evaluate medical/scientific information.
  • Excellent written and oral communication.
  • Experience with clinical trials and safety oversight.

Responsibilities

  • Accountable for safety across the study and provide medical advice for risk assessment.
  • Contribute to protocol design, regulatory documents and safety plans.
  • Monitor safety data and review SAEs and cumulative safety data.
  • Interact with regulatory authorities and key opinion leaders as needed.
  • Support study teams in data quality, manuscript and regulatory deliverables.

Skills

Clinical leadership
Risk assessment
Medical monitoring
Regulatory knowledge
AI tools awareness

Education

Medical degree (M.D./D.O. or equivalent)
Medical license to prescribe medicines
0-4 years' work experience

Job description

Pfizer seeks a Clinician within a vaccine development program in the United States. This role may serve as clinical lead for one or more studies, working closely with the global clinical program lead to ensure execution and accountability for design, monitoring, and reporting.

The clinician provides medical oversight for Clinical Trials, supports regulatory interactions, and ensures patient safety through risk assessment, safety reviews, and data interpretation across trial sites.

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