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8 дней назад

Medical Director, Clinical Development-Rheumatology (Rheumatology)

Формат работы
onsite
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
Medical Director, Clinical Development-Rheumatology (Rheumatology): Leading Phase 2 and Phase 3 rheumatology trials and translating clinical evidence into regulatory and development deliverables with an accent on trial design, medical oversight, data interpretation, and benefit-risk evaluation. Focus on leading cross-functional study teams, developing clinical and regulatory documents, and supporting immunology and autoimmune disease programs.

Location: Spring House, Pennsylvania, United States; additional job posting locations include Cambridge, Massachusetts, and San Diego, California. Domestic and international travel may be required.

Company

Johnson & Johnson MedTech develops healthcare solutions and medicines across Innovative Medicine and MedTech, including treatments for immunological disorders.

What you will do

  • Lead the design, execution, analysis, and reporting of Phase 2 and Phase 3 rheumatology clinical trials.
  • Serve as medical lead for assigned studies, overseeing eligibility guidance, medical monitoring, safety reviews, protocol deviations, and benefit-risk evaluations.
  • Lead cross-functional study teams, manage risks, drive decisions, and deliver study milestones.
  • Develop and review protocols, investigator brochures, clinical study reports, publications, and other clinical documents.
  • Contribute medical content to regulatory submissions, briefing packages, health authority responses, and regulatory interactions.
  • Interpret clinical, translational, and competitive evidence and build relationships with investigators, experts, patient organizations, and development partners.

Requirements

  • MD or equivalent medical degree.
  • Clinical expertise in rheumatology; board certification is preferred.
  • Experience leading or materially contributing to interventional clinical trials, including protocol development, medical monitoring, data review, and study reporting.
  • Typically 3 or more years of relevant clinical development or clinical research experience preferred, with pharmaceutical or biotechnology industry experience strongly preferred.
  • Strong knowledge of rheumatology, immunology, clinical trial methodology, and Good Clinical Practice.
  • Strong analytical, scientific writing, presentation, collaboration, and influencing skills, including experience in global, cross-functional, matrixed teams.

Nice to have

  • Experience with deep depletion approaches or chimeric antigen receptor T-cell therapy.
  • Academic clinical research experience.

Culture & Benefits

  • Inclusive, collaborative, and high-accountability work environment.
  • Opportunity to mentor clinical team members and contribute to immunology and autoimmune disease programs.
  • Retirement pension and 401(k) savings plan, subject to plan terms.
  • Eligibility for the long-term incentive program.
  • Paid vacation, sick time, holidays, parental leave, caregiver leave, bereavement leave, volunteer leave, and other time-off benefits.

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