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Medical Science Writing Manager - Onsite - Boston Seaport

Clear Point Consultants · Boston, MA, USA ·

Pay:
120.000
Job type:
Full Time

We’re looking for a Medical Science Writing Manager to lead the development and delivery of high-quality scientific and medical content across a variety of projects and audiences.

This is an ideal opportunity for an experienced medical/scientific writer who enjoys both hands-on writing and managing projects, stakeholders, and other writers .

What you’ll do:

  • Lead the development of medical and scientific content from concept through final delivery
  • Manage multiple writing projects, timelines, and priorities
  • Write, edit, and review scientific, medical, clinical, and educational materials
  • Translate complex scientific and clinical information into clear, compelling content
  • Partner with scientists, physicians, clinical teams, regulatory professionals, and other subject matter experts
  • Review scientific literature, clinical data, and research findings for accuracy and relevance
  • Establish and maintain high standards for scientific accuracy, consistency, and quality
  • Provide guidance, mentoring, and feedback to other medical/scientific writers
  • Coordinate reviews and approvals with cross-functional stakeholders
  • Ensure deliverables meet applicable scientific, regulatory, and quality requirements

What we’re looking for:

  • Bachelor’s, Master’s, or PhD in Life Sciences, Biomedical Sciences, Pharmacy, Medicine , or a related field
  • Several years of experience in medical writing, scientific writing, medical communications, clinical research, or a related area
  • Demonstrated experience leading projects and working with cross-functional teams
  • Excellent writing, editing, and proofreading skills
  • Strong understanding of scientific and medical terminology
  • Ability to interpret clinical data and scientific literature
  • Strong organizational skills and attention to detail
  • Experience mentoring or managing other writers is preferred

Experience in pharmaceutical, biotechnology, clinical research, regulatory writing, medical communications, or scientific publications is highly desirable.

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