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Medical Writing Pharmaceutical Jobs (NOW HIRING)

Hueman PE Talent Solutions

Medical Writer II

Belmont, MA · Remote

$55K - $65K/yr

Excellent writing skills * Previous relevant experience in medical writing, technical writing, scientific communications, pharmaceutical/biotech training, or a related field * Ability to develop ...

BioMarin Pharmaceutical Inc.

Senior Medical Writer

... the pharmaceutical industry - OR - at least 10 years of medical or scientific writing experience as a primary job responsibility. 1) Medical Writing: * Experience writing, reviewing, or editing ...

BioMarin Pharmaceutical Inc.

Senior Medical Writer

... the pharmaceutical industry - OR - at least 10 years of medical or scientific writing experience as a primary job responsibility. 1) Medical Writing: * Experience writing, reviewing, or editing ...

Precision Medicine Group, LLC.

$75K - $112K/yr

Writing/Editorial Division: Precision AQ Business Unit: Engagement Solutions Requisition Number ... Communicate medical content with internal team and pharmaceutical clients, as necessary * Attend ...

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As of Sep 12, 2026, the average hourly pay for medical writing pharmaceutical in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

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Infographic showing various Medical Writing Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Senior Director, Medical Writing

Burlington, MA • Hybrid

MBX Biosciences
Biotechnology Research and Development • 1 - 10 employees
Learn more about MBX Biosciencesexternal

Full-time

Posted 8 days ago

Job description

Position Summary

MBX Biosciences is seeking an experienced and dynamicSenior Director of Medical Writingto establish and lead our Medical Writing department. This full-time leadership role will be instrumental in building a high-performing team and developing robust processes to support clinical and regulatory documentation across the organization. The successful candidate will be responsible for overseeing the creation of high-quality clinical and regulatory documents, ensuring alignment with industry standards and global regulatory requirements. This role requires exceptional leadership, deep expertise in medical writing, and a collaborative mindset to work effectively across cross-functional teams, including Clinical Development, Regulatory Affairs, Quality, and Program Management. This individual will report directly to theSenior Vice President of Regulatory & Qualityand will play a key role in shaping the strategic direction of medical writing within the company.

 Key Responsibilities

  • Lead and manage the Medical Writing team (including internal and external writers), providing guidance, mentorship, and professional development opportunities.
  • Oversee the preparation, review, and submission of clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions.
  • Ensure all documents are accurate, scientifically sound, and compliant with regulatory guidelines and company standards.
  • Collaborate with clinical, regulatory, and scientific teams to gather and interpret data, ensuring clear and effective communication of complex scientific information.
  • Develop and implement medical writing processes, templates, and best practices to enhance efficiency and quality.
  • Stay current with industry trends, regulatory requirements, and best practices in medical writing.
  • Represent the Medical Writing function in cross-functional meetings and contribute to strategic planning and decision-making.
  • Manage timelines and resources to ensure timely completion of projects.
  • Other responsibilities as assigned.  

Qualifications

  • Advanced degree in life sciences, medical writing, or a related field (PhD, MD, or equivalent preferred).
  • 15+ years of medical writing experience in the biotechnology or pharmaceutical industry.
  • Proven track record of leading and managing a team of medical writers.
  • Extensive knowledge of regulatory requirements and guidelines (e.g., ICH, FDA, EMA).
  • Excellent written and verbal communication skills, with the ability to convey complex scientific information clearly and concisely.
  • Excellent problem-solving skills, strategic thinking, and ability to work in a fast-paced, collaborative environment.
  • Outstanding scientific leadership and collaboration skills.  
  • Outstanding interpersonal skills, self-awareness, and ability to manage team dynamics. 

Travel & In Office Presence 

You will be expected to travel periodically based on the needs of the business, including attendance at Together Weeks, Together Days, and functional meetings as requested by the team. Employees are expected to work on hybrid schedules, consistent with local office practices and the terms of the companies in office policy as in effect from time to time.

EEO Statement: 

MBX Biosciences is an Equal Opportunity Employer and is committed to treating all applicants fairly without discrimination. We welcome applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. 

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