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Director Medical Writing Publication Jobs (NOW HIRING)

Alkermes

Associate Director, Medical Writing

Waltham, MA · Hybrid

$175K - $190K/yr

The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities across one or more clinical development programs. This role combines hands-on ...

Travere

Associate Director, Medical Writing

OR · On-site +1

The Associate Director, Medical Writing is responsible for oversight and authoring (if needed) of regulatory submissions (Common Technical Documents [CTD]), as well as other regulatory, clinical, and ...

Alkermes

Associate Director, Medical Writing

Waltham, MA · On-site

$175K - $190K/yr

The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities across one or more clinical development programs. This role combines hands-on ...

Biogen

Director, Medical Writing - WCH

$191K - $263K/yr

As the Director of Medical Writing for the West Coast Hub (WCH) you are responsible for the writing and/or managing complex marketed and development programs at the portfolio level based on ...

Biogen

Director, Medical Writing - WCH

$191K - $263K/yr

As the Director of Medical Writing for the West Coast Hub (WCH) you are responsible for the writing and/or managing complex marketed and development programs at the portfolio level based on ...

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Director Medical Writing Publication information

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$76.5K

$177.2K

$304.5K

How much do director medical writing publication jobs pay per year?

As of Aug 20, 2026, the average yearly pay for director medical writing publication in the United States is $177,191.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,000.00 and $203,500.00 per year, depending on experience, location, and employer.

What does a director medical writing publication do?

A Director of Medical Writing Publication oversees the development, review, and delivery of scientific and clinical documents intended for publication in medical journals or presentation at conferences. They lead teams of medical writers, ensure adherence to regulatory and journal guidelines, and coordinate with cross-functional teams such as clinical, regulatory, and biostatistics. This role is responsible for setting publication strategies, managing timelines, and maintaining high standards of scientific accuracy and quality in all publications. Additionally, the director may interact with external authors and stakeholders to ensure that publication goals align with organizational objectives.

What are the key skills and qualifications needed to thrive as a director medical writing publication?

To thrive as a Director Medical Writing Publication, you need an advanced degree in life sciences or pharmacy, extensive experience in medical writing, and a deep understanding of scientific publication standards. Familiarity with document management systems, reference management software, and guidelines such as ICMJE and GPP is essential. Exceptional leadership, project management, and communication skills help in guiding teams and collaborating with cross-functional stakeholders. These skills ensure the delivery of high-quality, compliant publications that accurately represent scientific data and support organizational goals.

How does a director medical writing publication typically collaborate with cross-functional teams in the publication process?

A Director of Medical Writing Publication frequently works with clinical research, regulatory affairs, biostatistics, and medical affairs teams to ensure the accuracy, compliance, and timely delivery of scientific publications. This role involves leading publication strategy meetings, coordinating input from subject matter experts, and overseeing the development of manuscripts, abstracts, and presentations. Effective communication and project management skills are essential, as the director must align multiple stakeholders and ensure all deliverables meet both internal standards and external guidelines.

What is the difference between Director Medical Writing Publication vs Medical Writer?

AspectDirector Medical Writing PublicationMedical Writer
CredentialsAdvanced degrees (MD, PhD, PharmD), extensive experienceBachelor's or Master's degree in life sciences or related field
Work EnvironmentLeadership role in pharmaceutical or biotech companies, overseeing publication teamsIndividual contributor, preparing scientific documents
ResponsibilitiesStrategic planning, managing publication processes, team leadershipWriting, editing, and reviewing scientific publications

The main difference is that the Director Medical Writing Publication holds a leadership role overseeing publication strategies and teams, while the Medical Writer focuses on creating and editing scientific documents. The director typically has more experience, advanced degrees, and managerial responsibilities, whereas the medical writer is primarily involved in hands-on writing tasks.

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Director Medical Writing Publication jobs near you
Infographic showing various Director Medical Writing Publication 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 $177,191 per year, or $85.2 per hour.

Associate Director, Medical Writing

Calico

South San Francisco, CA • On-site

$230K - $240K/yr

Full-time

Re-posted 25 days ago

Job description

Who We Are:
Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico's highly innovative technology labs, its commitment to curiosity-driven discovery science and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs.
Position Description:
Calico is seeking an Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high quality clinical and regulatory documents, in compliance with applicable guidelines and regulations. The successful candidate should be able to effectively collaborate with cross-functional representatives, collaboration partners, external vendors, and stakeholders while maintaining a positive team environment. This role will function as a strong project manager and technical leader with demonstrated scientific and stakeholder-focused leadership skills.
Key Responsibilities:
  • Document Leadership and Authoring:
    • Provides medical writing leadership for clinical programs
    • Acts as a medical writing subject matter expert and collaborates with the Clinical Science team to deliver on clinical documents including clinical study protocols and protocol-related documents (e.g. informed consent forms), clinical study reports, DSURs, Investigator's Brochures, IND clinical summaries/overviews, and CTD components (e.g. Module 2 summaries)
    • Partners with the regulatory function to ensure timely completion of high-quality regulatory documents including health authority meeting requests, briefing packages, responses to requests for information, and other documents as required for submissions
  • Vendor Management: Provides guidance to external writers on prioritization, content and timeline development, and process management to support clinical development and regulatory activities
  • Process Improvement:
    • Develops medical writing best practices (e.g. standard timelines, clinical document templates, Calico Style Guide)
    • Partners with the Quality Assurance team to develop new and update existing Standard Operating Procedures for Medical Writing processes and all clinical documents to ensure compliance with ICH requirements
Position Requirements:
  • Master's degree in a life science discipline from an accredited college or university; PharmD or PhD preferred
  • Minimum of 8+ years of scientific or medical writing experience at a biotech/ pharmaceutical company or clinical research organization setting
  • Expert knowledge of standard clinical regulatory document types and associated regulatory requirements (e.g. ICH guidance, FDA, EMA, Health Canada, Asia-Pacific regulations, etc.)
  • Prior writing experience in Clinical Study Protocols, Clinical Study Reports, DSUR, Investigator's Brochures, IND clinical summaries/overviews, CTD clinical summaries, and partnering with external investigators to support Investigator Initiated Study Trials
  • Expert ability of Microsoft Office Suite, Adobe Acrobat, collaborative review management systems (e.g. SharePoint) and documents management (e.g. Veeva RIM)
  • Experience in resource planning and management experience of contractors
  • Excellent organization skills with a passion for delivering quality results
  • Detail-oriented mindset with excellent verbal and written communication skills
  • Self-motivated and able to work collaboratively
  • Ability to "roll up sleeves" in a start-up environment and a positive can-do attitude
  • Must be willing to work onsite at least 4 days a week

The estimated base salary range for this role is $230,000 - $240,000. Actual pay will be based on a number of factors including experience and qualifications. This position is also eligible for two annual cash bonuses.

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