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4 часа назад

Associate Director, Global Medical Affairs Publication Operations (MedTech)

137 000 - 235 750$
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
Associate Director, Global Medical Affairs Publication Operations (MedTech): Producing and overseeing scientific publications, including abstracts, posters, presentations, manuscripts, and letters to editors, with an accent on publication planning, medical writing, and compliance. Focus on interpreting scientific data, coordinating authors and writers, managing publication workflows, and applying Good Publication Practice and related standards.

Location: Raritan, New Jersey, United States of America; up to 10% travel.

Annual base pay: $137,000–$235,750, plus eligibility for performance-based bonuses and long-term incentives.

Company

Johnson & Johnson MedTech develops healthcare solutions and medical technologies designed to improve patient outcomes.

What you will do

  • Write, review, edit, and oversee the production of abstracts, posters, oral presentations, manuscripts, and letters to editors.
  • Execute publication plans by assigning medical writers and coordinating editing, project management, and delivery to author teams.
  • Interpret data and source documents and support the development of tables, figures, and publication materials.
  • Coordinate kick-off meetings and collaborate with internal and external authors, product teams, and other stakeholders.
  • Provide subject-matter expertise on publication policies, SOPs, Good Publication Practice, ICMJE, CONSORT, and AMA style standards.
  • Maintain publication templates, style guides, workflow tools, and review and approval systems.

Requirements

  • PhD, PharmD, MD, or equivalent degree with at least 8 years of relevant pharmaceutical or scientific experience, or a Master’s or other advanced degree with at least 10 years of relevant experience.
  • Demonstrated ability to interpret and organize scientific data.
  • Ability to work independently and collaboratively while managing multiple documents and projects.
  • Experience with medical writing document standards and processes is preferred.
  • Experience with workflow management tools such as JPUBS, Datavision, or PubSTRAT is preferred.
  • CMPP certification, project management experience, and knowledge of oncology, neuroscience, or immunology are preferred.

Culture & Benefits

  • Inclusive work environment guided by the company’s Credo.
  • Medical, dental, vision, life, disability, business accident, and group legal insurance may be available.
  • Eligibility for pension and 401(k) savings plans.
  • Vacation, sick time, holidays, and Work, Personal and Family Time benefits.
  • Annual performance bonus and long-term incentive program eligibility.

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