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Senior Director, Clinical Lead - Neuropsychiatry

232 000 - 401 350$
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
Senior Director, Clinical Lead - Neuropsychiatry (Clinical Drug Development): Developing and executing late-phase clinical strategies and trials for neuropsychiatric treatments with an accent on clinical development plans, medical monitoring, regulatory submissions, and cross-functional leadership. Focus on designing Phase II/III studies, interpreting safety and efficacy data, preparing global health authority filings, and managing clinical program budgets.

Location: Hybrid role based in Titusville or Raritan, New Jersey; Spring House, Pennsylvania; or Cambridge, Massachusetts, United States

Base pay: $232,000–$401,350 per year

Company

Johnson & Johnson MedTech develops healthcare innovations, medicines, medical technologies, and patient-focused solutions across complex diseases.

What you will do

  • Develop and execute medical and scientific strategies and clinical development plans for late-phase compounds.
  • Lead cross-functional Clinical Teams and manage project physicians and other medical staff.
  • Own clinical trial design, clinical study reports, medical monitoring, safety activities, and Independent Data Monitoring Committee materials.
  • Interpret clinical research results and support global regulatory submissions, health authority interactions, publications, and advisory committee presentations.
  • Assist with regulatory strategies, product evaluation, labeling, surveillance, early clinical development, and assessment of new scientific opportunities.
  • Manage budgets for project-related clinical activities.

Requirements

  • MD or international equivalent in a relevant area, with appropriate post-doctoral training and certification.
  • At least 5 years of clinical research or pharmaceutical industry experience, including at least 3 years of Phase II/III development experience in industry.
  • At least 3 years of successful managerial, supervisory, or related experience.
  • Expertise in clinical drug development, clinical development planning, Good Clinical Practices, and clinical-trial regulatory requirements.
  • Experience working in a matrix environment and collaborating with clinical operations, medical affairs, marketing, regulatory affairs, and other functions.
  • Fluent written and spoken English required.

Nice to have

  • Board certification or eligibility in psychiatry or neurology.
  • Global registration experience and experience interacting with health authorities.
  • Experience in neuroscience, neuropsychiatry, clinical research, regulations, data management, or informatics.

Culture & Benefits

  • Patient-focused work addressing complex neurological and psychiatric diseases.
  • Inclusive work environment guided by the company’s Credo.
  • Eligibility for pension and 401(k) savings plans.
  • Vacation, sick time, holidays, personal and family time, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time-off benefits.

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