Назад
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20 часов назад

Associate Director, Aesthetics Clinical Development

141 500 - 268 500$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
c1
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, Aesthetics Clinical Development (Clinical Trials/Medical Devices): Designing and executing clinical development plans and trials for aesthetics products with an accent on scientific validity, safety and efficacy data, and regulatory requirements. Focus on interpreting clinical data, coordinating cross-functional teams, overseeing registration-track studies, and preparing clinical content for regulatory submissions and publications.

Location: Irvine, California, United States; hybrid schedule with 3 days in the office

Salary: $141,500–$268,500 per year

Company

hirify.global develops medicines and solutions across immunology, oncology, neuroscience, and Allergan Aesthetics.

What you will do

  • Design clinical development plans spanning early translational development through mature product life-cycle strategies.
  • Design, conduct, report, and interpret clinical trials supporting regulatory and commercial strategies.
  • Review accumulating safety and efficacy data, protocol deviations, and the scientific integrity of clinical content.
  • Coordinate with Clinical Operations on study enrollment, timelines, and key deliverables.
  • Lead cross-functional sub-teams and collaborate with medical affairs, commercial, statistics, regulatory, discovery, and clinical operations stakeholders.
  • Support investigator education, regulatory submissions, scientific publications, and external scientific meetings.

Requirements

  • Advanced education such as MD, DO, PhD, PharmD, or MA with relevant experience is preferred.
  • At least 7 years of clinical development experience is typically required.
  • Experience designing and executing registration-track clinical protocols leading to regulatory submission.
  • Knowledge of clinical-trial regulatory requirements and experience with US and global regulatory bodies.
  • Strong cross-functional collaboration skills and excellent oral and written English communication skills.
  • Experience in international markets; experience developing novel aesthetics medical devices is highly desirable.

Culture & Benefits

  • Hybrid work arrangement with three office days per week in Irvine.
  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) and participation in long-term incentive programs for eligible employees.
  • Opportunities to mentor junior team members and participate in R&D and Clinical Development process improvement.

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