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Health Care 🏢 Full Time ⭐️ Verified

Senior Medical Writer

MedTech Solutions
Boston
Salary Estimate
USD 120.000 – USD 160.000
Live Update
18 Mei 2026
Deadline
18 Mei 2027

Job Description

Are you a master of scientific storytelling? MedTech Solutions is seeking a highly skilled Senior Medical Writer to join our elite Boston-based team. In this pivotal role, you will bridge the gap between complex clinical data and accessible healthcare communication, driving our mission to improve patient outcomes through precision medicine.

Join a culture that values curiosity, rigor, and innovation. We offer a competitive compensation package, comprehensive benefits, and a collaborative environment where your expertise will directly influence the future of medical science.

Why Join Us?

  • Work with world-class scientists and thought leaders.
  • Access to state-of-the-art writing tools and resources.
  • Flexible hybrid work model supporting work-life balance.

Ready to elevate healthcare communication? Apply today.

Responsibilities

  • Lead the end-to-end writing process for high-impact deliverables, including clinical study reports (CSRs), protocols, and medical journal manuscripts.
  • Synthesize complex clinical trial data into clear, concise, and scientifically accurate narratives for diverse audiences, including regulatory bodies and healthcare professionals.
  • Ensure strict adherence to regulatory standards (FDA, EMA, ICH) and internal style guides to maintain the highest quality and compliance.
  • Collaborate with cross-functional teams, including medical directors, clinical operations, and regulatory affairs, to align content with strategic objectives.
  • Conduct thorough literature reviews and peer reviews to ensure accuracy and integrity of all scientific content.
  • Present key findings and insights at internal review meetings and external conferences.

Qualifications

  • Advanced degree in Life Sciences (MD, PhD, PharmD) or equivalent clinical research experience.
  • Minimum of 5 years of professional experience in medical writing within the pharmaceutical or biotechnology industry.
  • Proven track record of authoring successful regulatory submissions or peer-reviewed publications.
  • Expertise in medical writing software (e.g., Author-it, AuthorGen) and familiarity with Document Management Systems.
  • Exceptional command of the English language, with a keen eye for detail and grammar.
  • Strong ability to manage multiple projects simultaneously in a fast-paced, deadline-driven environment.

Required Skills

Medical Writing Regulatory Affairs Clinical Research Life Sciences Data Analysis Storytelling Peer Review Protocols Clinical Study Reports

Ready to Take on This Challenge?

Make sure your resume is ready. Submit your application now before the deadline.

Apply Now

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