Clinical Development Medical, Associate Director (Pearl River)

Location: Pearl River, New York, United StatesCompany: PfizerPosted: 2026-07-24Clinician Role in Pfizer Vaccine Development ProgramThe primary purpose is to serve as a Clinician within a Pfizer vaccine development program. This role may serve as a clinical lead for one or more studies within a clinical program and works closely with the global clinical program lead who is ultimately responsible for execution of the overall 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.The clinician is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies and to ensure patient safety.Role Responsibilities:Accountable for safety across the studyProtocol design and strategySupport study teamSupports the program teamInteract with regulatory authorities, key opinion leaders, and principal investigatorsBasic Qualifications: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) and has utilized the license to prescribe medicines in a patient care setting for an aggregate duration of at least two years.0-4 years' work experiencePossesses 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 environmentPreferred Qualifications: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.Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.Additional Details:Last date to apply is July 25, 2026Work Location Assignment: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.