Medical Science Writing Manager - Onsite - Boston Seaport

Clear Point Consultants; Boston (MA); On-site; USD 120,000 - 160,000; Full time

Job summary

Clear Point Consultants is seeking a Medical Science Writing Manager in Boston to lead the creation and delivery of high-quality scientific content across diverse projects. The role combines hands-on writing with managing timelines, stakeholders, and a team of writers.

You will translate complex clinical data into clear materials, collaborate with scientists, clinicians, and regulatory colleagues, and uphold stringent scientific standards. Mentoring junior writers is also a key responsibility.

Qualifications

• Minimum several years of medical writing or scientific communications experience.
• Experience leading projects and cross-functional teams.
• Strong writing, editing, and proofreading skills.

Responsibilities

• Lead development of medical/scientific content from concept to delivery.
• Manage multiple writing projects, timelines, and priorities.
• Write, edit, and review scientific, medical, clinical, and educational materials.
• Translate complex information into clear, compelling content.

Skills

Medical writing

Project management

Team leadership

Stakeholder management

Education

Bachelor’s/Master’s/PhD in Life Sciences

Tools

MS Word

Reference management

Job description

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.