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2 дня назад

Clinical Development Medical, Associate Director

189 200 - 315 400$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Clinical Development Medical, Associate Director (Clinical Trials/Vaccine Development): Providing medical and scientific oversight for Pfizer vaccine clinical studies, with an accent on patient safety, protocol design, regulatory documentation, and clinical data interpretation. Focus on monitoring safety data, guiding study teams, supporting regulatory interactions, and delivering high-quality clinical study reports.

Location: Pearl River, New York, United States; hybrid work required, with on-site attendance an average of 2.5 days per week

Annual base salary: $189,200–$315,400, plus a 22.5% bonus target and potential long-term incentive participation.

Company

hirify.global develops medicines and vaccines and conducts global clinical development programs.

What you will do

  • Serve as a clinician and potential clinical lead for one or more vaccine development studies.
  • Provide medical oversight for study design, execution, monitoring, delivery, reporting, and patient safety.
  • Review individual and cumulative safety data, support adverse-event assessments, and participate in safety review teams.
  • Contribute medical input to protocols, clinical development plans, monitoring guidelines, statistical analysis plans, and informed consent documents.
  • Support study teams with data interpretation, investigator training, vendor coordination, issue resolution, closeout, audits, and inspection readiness.
  • Contribute to regulatory documents, clinical study reports, publications, and interactions with regulatory authorities, key opinion leaders, and principal investigators.

Requirements

  • Medical degree (M.D., D.O., or equivalent).
  • At least one year of independent prescribing licensure after internship or housemanship and at least two years of licensed patient-care prescribing experience.
  • 0–4 years of professional work experience.
  • Ability to critically evaluate medical and scientific information and understand clinical program and study design, development, and execution.
  • Excellent written and oral communication skills and the ability to adapt to a fast-paced, changing environment.
  • Must be authorized to work permanently in the United States by any employer; visa sponsorship is not available.

Nice to have

  • Knowledge or documented work experience in statistics.
  • Training or experience in infectious diseases or hospital infection control.
  • Experience with investigational clinical trials.

Culture & Benefits

  • Hybrid work arrangement with regular on-site collaboration.
  • Participation in the Global Performance Plan and potential share-based long-term incentives.
  • 401(k) matching and an additional retirement savings contribution.
  • Paid vacation, holidays, personal days, caregiver or parental leave, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.
  • Relocation assistance may be available based on business needs and eligibility.

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