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8 дней назад

Preclinical Evidence & External Partnerships Associate Director

137 000 - 235 750$
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
Preclinical Evidence & External Partnerships Associate Director (Medical Affairs/MedTech): Developing pre-market evidence strategies, preclinical protocols, and external physician research partnerships for electrophysiology and cardiovascular product programs with an accent on clinically relevant evidence generation, regulatory requirements, and scientific publication planning. Focus on leading preclinical scientists, coordinating external studies, supporting first-in-human use, and delivering research programs within budget and compliance requirements.

Location: Irvine, California, United States; hybrid work model

Base pay: $137,000–$235,750 per year

Company

Johnson & Johnson MedTech develops healthcare technologies and personalized, less invasive treatments across cardiovascular care, electrophysiology, stroke, and heart recovery.

What you will do

  • Develop preclinical evidence strategies supporting first-in-human use across portfolio programs.
  • Manage the preclinical external research program and physician partnerships with cross-functional clinical science partners.
  • Review study proposals and coordinate timely execution of approved studies with external stakeholders.
  • Use program data and metrics to review progress and provide leadership updates.
  • Support evidence dissemination, publication planning, and identification of research gaps.
  • Contribute scientific input to publications, preclinical protocols, and external physician research plans.

Requirements

  • Bachelor’s degree in Biological Science or a related discipline required; a Master’s or PhD is strongly preferred.
  • At least 8 years of related scientific and technical experience, including leadership or management experience in Medical Affairs or a similar function.
  • At least 2 years of people management experience required.
  • Expertise in preclinical science and processes, product development, healthcare trends, clinical trial regulations, and team dynamics.
  • Ability to lead preclinical scientists and provide strategic and scientific input across new product development projects.
  • Up to 25% domestic and international travel may be required.

Nice to have

  • Experience in cardiovascular, electrophysiology, or structural heart.
  • Experience supporting global regulatory submissions for medical devices, biologics, or drugs, including IDE, 510(k), De Novo, or PMA submissions.

Culture & Benefits

  • Inclusive work environment focused on individual dignity, diversity, and merit.
  • Vacation, sick time, holiday pay, and work, personal, and family time.
  • Parental, bereavement, caregiver, volunteer, and military spouse leave programs.
  • Work supporting innovative cardiovascular and electrophysiology treatments designed to improve patient care.

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