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7 дней назад

Clinical Pharmacology Lead (MIDD)

106 000 - 176 600$
Формат работы
hybrid
Тип работы
fulltime
Грейд
lead
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 Pharmacology Lead (MIDD): Leading clinical pharmacology and model-informed drug development strategies for Pfizer’s Internal Medicine portfolio with an accent on PK/PD modeling, dose selection, study design, and regulatory submissions. Focus on designing end-to-end MIDD plans, integrating pharmacokinetics, pharmacodynamics, patient characteristics, and disease states, and guiding multifunctional teams through clinical development.

Location: Cambridge, Massachusetts, 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. Permanent U.S. work authorization is required; visa sponsorship is not available.

Salary: $106,000–$176,600 annual base salary, plus a 15% bonus target and eligibility for a share-based long-term incentive program.

Company

hirify.global is a pharmaceutical company developing medicines through clinical research, model-informed drug development, and cross-functional scientific collaboration.

What you will do

  • Represent Clinical Pharmacology on clinical subteams, development teams, and other multifunctional project teams.
  • Lead clinical pharmacology expertise, deliverables, and best practices across assigned Internal Medicine projects.
  • Design and execute clinical pharmacology plans, including PK/PD analyses, immunogenicity and biomarker strategies, and clinical development plans.
  • Plan and oversee study-level activities such as protocol authoring, clinical phase oversight, reporting, and dose-range finding.
  • Develop and implement end-to-end MIDD plans using innovative analytical methods to optimize doses, dosage regimens, and study designs.
  • Contribute to regulatory documents and interactions, and represent the organization through publications, presentations, scientific societies, and industry consortia.

Requirements

  • Strong quantitative skills and expertise in mechanistic PK/PD modeling, systems pharmacology, literature meta-analyses, population modeling, and clinical trial simulations.
  • Experience with tools such as NONMEM and R.
  • M.D./Ph.D. or equivalent training and experience in pharmacokinetics, pharmacometrics, clinical pharmacology, engineering, or a related discipline; 0+ years of industry experience accepted.
  • Pharm.D. or equivalent training and experience in a related discipline, with 2+ years of industry experience.
  • Excellent written and verbal communication, presentation skills, and the ability to influence and collaborate across disciplines.
  • Ability to work in global team meetings across different time zones and maintain permanent U.S. work authorization.

Culture & Benefits

  • Collaborative, multifunctional environment focused on innovative clinical pharmacology and MIDD methods.
  • Opportunities for learning, professional growth, scientific publications, presentations, and external representation.
  • 401(k) plan with hirify.global matching contributions and an additional retirement savings contribution.
  • Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.

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