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5 часов назад

Vice President, Clinical Pharmacology

Тип работы
fulltime
Грейд
head
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
Vice President, Clinical Pharmacology (Drug Development): Providing strategic and operational leadership for clinical pharmacology services supporting biological and small-molecule development with an accent on regulatory strategy, scientific writing, and client delivery. Focus on designing clinical pharmacology programs, preparing FDA meeting materials and regulatory submissions, developing the organization, and driving service growth.

Location: United States of America

Company

hirify.global supports biotech, medtech, and specialty pharmaceutical companies in developing medicines, medical devices, and diagnostics.

What you will do

  • Provide strategic and operational leadership for the clinical pharmacology team, including planning, budgeting, recruiting, and team development.
  • Oversee the design, delivery, scope, budgets, and proposals for integrated and standalone clinical pharmacology services.
  • Develop organizational capabilities, including contractor networks, to support comprehensive service delivery.
  • Monitor industry trends and operational performance while developing plans for revenue and gross-margin growth.
  • Support clients and project teams through consulting work, FDA and regulatory health authority meetings, data review, protocol design, and regulatory submission authoring and review.
  • Represent hirify.global in the scientific community and marketplace, contribute to business development and thought leadership, and advise the Consulting Leadership Team.

Requirements

  • Ph.D. in pharmacology, pharmaceutical sciences, PharmD, or a related discipline.
  • 10–15 years of experience in clinical pharmacology studies or programs involving biologicals and small molecules within a CRO, pharmaceutical, biotechnology, or related environment.
  • Knowledge of 505(b)(2) programs and regulatory requirements for biologics, gene therapy, and/or vaccines.
  • Demonstrated research experience, scientific writing and editing skills, and the ability to analyze scientific and technical literature.
  • Effective written and spoken English communication is required.
  • Availability for a flexible schedule and 10–15% travel, including inter-office travel.

Nice to have

  • Board certification in Clinical Pharmacology, such as DABPC (AP).

Culture & Benefits

  • Flexibility and balance to support personal and professional needs.
  • Opportunities to develop skills and advance professionally.
  • Collaborative work with global companies, sponsors, consulting teams, and clinical development functions.
  • Participation in scientific conferences, industry events, and thought leadership activities.

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