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Director Medical Writing Publication Jobs (NOW HIRING)

Director, Medical Writing

Plainsboro, NJ

$198K - $297K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Role: The Director, Medical Writing is responsible for advancing the medical writing portfolio ... publications (abstracts, posters, slide presentations, and manuscripts). Team Leadership and ...

The Director, Medical Writing will be responsible for authoring, reviewing, and managing a broad range of clinical and regulatory documents while helping establish and scale medical writing processes ...

Job Summary (Primary function) The Director, Medical Writing is responsible for the medical writing activity within a portfolio of programs. Ensures oversight of the development of the clinical ...

Director, Medical Writing

Waltham, MA · On-site

$220K - $235K/yr

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

Director, Medical Writing

Waltham, MA · Hybrid

$220K - $235K/yr

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

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Director Medical Writing Publication information

See salary details

$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.

More about Director Medical Writing Publication jobs

What cities are hiring for Director Medical Writing Publication jobs?

Cities with the most Director Medical Writing Publication job openings:

What states have the most Director Medical Writing Publication jobs?

States with the most job openings for Director Medical Writing Publication jobs include:

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 - Publications

System One

Raritan, NJ • Remote

$160K - $170K/yr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 25 days ago


Job description

Job Title: Associate Director, Medical Writing - Publications Work Model: Remote Hours: 40.0 Compensation: $160,000 - $170,000 Type: Salaried

Responsibilities

  • Provide expert writing and editing support to ensure timely production of high-quality documents (abstracts, posters, slide presentations, manuscripts, letters to editor, etc.) for publication in medical/scientific journals or presentation at meetings.
  • Manage and/or review and interpret data and source documents for information required for publication.
  • Assist in table and figure mock-up development.
  • Actively engage internal and external authors and other key stakeholders in the development of publication plans and strategy at the individual dataset, study, and/or compound level.
  • Skillfully manage projects through publication review system.
  • Provide direction, oversight, and editing for outsourced medical writers and project management of selected therapeutic area publications.

Requirements

  • A PhD, MD, or PharmD with a minimum of 5 years of relevant pharmaceutical/scientific experience is required OR a Master’s (or other advanced degree) with a minimum of 8 years relevant pharmaceutical/scientific experience is required
  • Research experience (including compilation of research reports or publications) in academia or the pharmaceutical industry or as part of a PhD, PharmD or postdoctoral program is preferred
  • Demonstrated ability to interpret and organize clinical and scientific data is required
  • Experience with MS Office Suite (Excel, Word, PowerPoint) is required
  • The ability to work well independently as well as part of a team is required
  • Project management experience is preferred
  • The ability to stay organized, manage time, and work on multiple documents/projects at once is required
  • Knowledge in across several therapeutic areas including immunology, neuroscience and/or oncology is preferred

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#LI-AD3 Ref: #568-Clinical


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About System One

Sourced by ZipRecruiter

System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US