Pfizer

Pfizer

Clinical Development Medical, Associate Director

United States - New York - Pearl River · Director

Sponsorship not specified$189k-$315kDetected 7 days ago
StatisticsAccessibilityRecruitingClinical TrialsClinical ResearchPatient CareResearchLeadershipCollaborationPublic Speaking

About the role

  • ROLE SUMMARY: The primary purpose is to serve as a Clinician within a Pfizer vaccine development program.
  • Importantly, this role will be set within a matrix team in executing studies, performing medical monitoring, supporting regulatory interaction, and taking on a leadership role in study teams for many of the clinical deliverables.
  • As appropriate, the clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP.

Responsibilities

  • Protocol design and strategy
  • Support study team
  • Support study team in issues resolution, study closeout, audit responses, inspection readiness, etc.
  • Supports the program team
  • May support Clinical Regulatory Authority interactions accountable for providing responses.
  • Liaise with Key Opinion Leaders and Principal Investigators in countries to build a Key Opinion Leaders /Principal Investigators network for new trials.

Requirements

  • 0-4 years' work experience
  • Interacts with DMCs and steering committees as required.

Nice to have

  • Documented work experience/knowledge of statistics.
  • Training and experience in infectious diseases and/or infection control in the hospital setting is preferred.
  • Experience with investigational clinical trials is preferred.
  • No pharmaceutical industry experience required.
  • Last date to apply is July 25, 2026
  • Relocation assistance may be available based on business needs and/or eligibility.
  • Candidates must be authorized to be employed in the U.S. by any employer.
  • U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

Compensation

  • Under supervision (Director/Sr. Director) authors clinical sections of regulatory documents (Investigator Brochure, Annual Reports, Investigational New Drug sections, clinical study report).
  • The annual base salary for this position ranges from $189,200.00 to $315,400.00.

Benefits

  • Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com).
  • Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.
  • These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure.
  • In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 22.5% of the base salary and eligibility to participate in our share based long term incentive program.
  • We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments.
  • Pfizer compensation structures and benefit packages are aligned based on the location of hire.

Visa & Work Authorization

  • U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

This listing is sourced directly from Pfizer's careers page and normalized into a canonical job model.