Назад
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21 час назад

Associate Director, Clinical Pharmacology

139 100 - 231 900$
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
Associate Director, Clinical Pharmacology (MIDD): Leading clinical pharmacology and model-informed drug development plans for Pfizer’s Internal Medicine portfolio with an accent on PK/PD modeling, dose optimization, and regulatory strategy. Focus on designing clinical studies, integrating patient and disease data into predictive models, and guiding cross-functional teams through drug development decisions.

Location: New York City, United States; hybrid role requiring residence within commuting distance and on-site work an average of 2.5 days per week or more as needed.

Annual base salary: $139,100–$231,900, plus a 17.5% bonus target and eligibility for a share-based long-term incentive program.

Company

hirify.global is a pharmaceutical company developing medicines through clinical research and model-informed drug development.

What you will do

  • Represent Clinical Pharmacology on clinical sub-teams, development teams, and other multifunctional project teams.
  • Design and execute clinical pharmacology plans and deliverables for Internal Medicine projects.
  • Plan and oversee PK/PD analyses, immunogenicity and biomarker strategies, study protocols, clinical phase activities, and reporting.
  • Develop dose-ranging strategies and optimize doses, dosage regimens, and study designs using quantitative pharmacology.
  • Lead end-to-end MIDD plans and contribute to regulatory documents, including IND, NDA/MAA, investigator’s brochures, briefing documents, and regulatory responses.
  • Develop new methodologies, collaborate with external experts, coach colleagues, and represent the field through publications and presentations.

Requirements

  • MD, PhD, PharmD, or equivalent training and experience in pharmacokinetics, pharmacometrics, clinical pharmacology, engineering, or a related discipline.
  • At least 5 years of industry experience in clinical pharmacology, clinical PK/PD, pharmacometrics, or systems pharmacology.
  • Strong quantitative expertise in mechanistic PK/PD modeling, systems pharmacology, population modeling, literature meta-analyses, and clinical trial simulations.
  • Experience with NONMEM, R, or comparable quantitative pharmacology tools.
  • Knowledge of drug development and quantitative approaches to knowledge integration, along with strong written, verbal, and presentation skills.
  • Permanent authorization to work in the United States is required; U.S. work visa sponsorship is not available now or in the future.

Nice to have

  • Experience developing methodologies through collaboration with external experts and scientific organizations.
  • Ability to attend global meetings periodically across different time zones.

Culture & Benefits

  • Hybrid work arrangement with regular on-site collaboration.
  • Comprehensive medical, prescription drug, dental, and vision coverage.
  • 401(k) plan with matching contributions and an additional retirement savings contribution.
  • Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
  • Relocation assistance may be available based on business needs and eligibility.

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