Associate Director, Vaccine Clinical Development

Pfizer

New York (NY)

Hybrid

USD 189.000 - 315.000

Vollzeit

Vor 13 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

401(k) match
Paid time off
Health benefits
Relocation assistance

Zusammenfassung

Pfizer is seeking a Clinician to lead medical oversight in a Pfizer vaccine development program. This role includes serving as a clinical lead for studies, ensuring patient safety, and working within a matrix team to monitor and report on trial activities.

Responsibilities cover safety reviews, protocol input, regulatory interactions, and collaboration with cross-functional teams to deliver high-quality clinical deliverables and reports.

Qualifikationen

  • Medical degree required and licensed to prescribe medicines.
  • 0-4 years' work experience.
  • Ability to critically evaluate medical/scientific information.
  • Strong written and oral communication skills.
  • Familiarity with clinical trial design and regulatory processes.
  • Experience with AI tools for problem solving and productivity.

Aufgaben

  • Provide medical oversight across studies, ensuring patient safety and regulatory compliance.
  • Contribute to protocol development, regulatory documents, and clinical plans.
  • Monitor safety data and participate in safety review activities with the team.
  • Collaborate with CROs/vendors to ensure data integrity and study timelines.
  • Lead or support dissemination of protocol-specific training and scientific reporting.

Kenntnisse

Medical knowledge
Clinical monitoring
Regulatory awareness
AI tools familiarity
Communication skills

Ausbildung

Medical degree (M.D./D.O.)

Tools

IRB/IEC review

Jobbeschreibung

Pfizer is seeking a Clinician to lead medical oversight in a Pfizer vaccine development program. This role includes serving as a clinical lead for studies, ensuring patient safety, and working within a matrix team to monitor and report on trial activities.

Responsibilities cover safety reviews, protocol input, regulatory interactions, and collaboration with cross-functional teams to deliver high-quality clinical deliverables and reports.

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