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Director Medical Writing Jobs in Washington (NOW HIRING)

MJH Life Sciences

Medical Writer

Washington, DC

$85K - $100K/yr

You'll work closely with scientific directors, editors, designers, and subject matter experts to ... This is more than writing -- it's about shaping content that informs, educates, and drives ...

New

MJH Life Sciences

Medical Writer

Washington, DC

$85K - $100K/yr

You'll work closely with scientific directors, editors, designers, and subject matter experts to ... This is more than writing -- it's about shaping content that informs, educates, and drives ...

New

Otsuka

Director, Global Clinical Development

Rockville, MD · On-site +1

$209K - $313K/yr

Otsuka is seeking an Director, Global Clinical Development (GCD) based remotely or in our Princeton ... medical writing. * Complete understanding of the global regulatory requirements. Demonstrated ...

Compass Health Center

Medical Director

Falls Church, VA · On-site

At the heart of Compass, our Medical Directors are entrusted with overseeing the implementation of ... Writing psychiatric clinical records to document all patient contact * Participating in Utilization ...

Heartland Hospice

Medical Director

Fairfax, VA · On-site

$218K - $272K/yr

We are seeking a dedicated Hospice Medical Director to join our leadership team and provide expert ... Excellent verbal and written communication skills. Personal Traits: * Passion for providing ...

Cape Fox Corporation

Medical Director

Washington, DC · On-site

Job Title Medical Director Cape Fox subsidiary, Wolf Lake Services, is seeking a highly organized ... Approve and periodically review written clinical protocols, standing orders, and referral pathways

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Director Medical Writing information

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$14.7K

$263.2K

$404.3K

How much do director medical writing jobs pay per year?

As of Aug 31, 2026, the average yearly pay for director medical writing in Washington is $263,180.00, according to ZipRecruiter salary data. Most workers in this role earn between $224,300.00 and $322,200.00 per year, depending on experience, location, and employer.

What is a director medical writing?

A Director of Medical Writing oversees the development of clinical and regulatory documents for pharmaceutical, biotech, or healthcare companies. They lead medical writing teams, ensuring high-quality, compliant, and scientifically accurate content for submissions, publications, and regulatory filings. This role involves collaborating with cross-functional teams, managing timelines, and maintaining adherence to industry guidelines. Strong leadership, project management, and writing expertise are essential for success in this position.

What are the responsibilities of a director of medical writing?

A director of medical writing works to write clinical documents, regulatory submission documents, manuals, research grant applications, and other technical medical publications. In this career, your duties include working to manage a team of writers and editors. You may also have author responsibilities yourself. Your employer may expect you to review documents written by other staff members and make or recommend changes. As the director of medical writing, you also create strategies for document writing and implement writing standards plans so that all employees know how to organize their documents to the same standard.

What are the typical daily responsibilities of a director medical writing?

A Director Medical Writing typically oversees a team of medical writers, ensuring the timely creation and quality of clinical and regulatory documents such as study protocols, clinical study reports, and submission dossiers. They collaborate closely with cross-functional teams including clinical operations, regulatory affairs, and biostatistics to align on project goals and timelines. In addition to managing and mentoring staff, they may also review and approve key documents, provide strategic input on document planning, and interact with clients or health authorities. This leadership role often involves balancing multiple projects simultaneously and problem-solving to navigate evolving industry requirements.

What are the key skills and qualifications needed to thrive in the director medical writing position, and why are they important?

To excel as a Director Medical Writing, you need advanced scientific expertise, strong leadership experience, and a background in life sciences or pharmacy, often supported by an advanced degree (PhD, PharmD, or MD). Familiarity with document management systems, regulatory submission platforms (such as eCTD), and certifications like the American Medical Writers Association (AMWA) are highly valued. Superior communication, strategic thinking, project management, and mentoring skills distinguish top performers in this position. These competencies ensure the production of high-quality documents, effective team leadership, and successful navigation of complex regulatory environments.

Do medical writers make good money?

Medical writers, including those in director roles, typically earn competitive salaries that vary by experience, location, and industry sector. Senior positions often offer higher compensation, and proficiency in regulatory guidelines and scientific knowledge can influence earning potential. Overall, medical writing can be a financially rewarding career path for qualified professionals.

Is there a demand for director medical writers?

There is a strong demand for director medical writers due to the growth of the pharmaceutical, biotech, and healthcare industries. These professionals are needed to lead medical writing teams, develop regulatory documents, and ensure compliance with industry standards, often requiring advanced degrees and experience in scientific communication. The role is expected to remain vital as regulatory requirements and the need for clear scientific communication increase.

What does a director of medical writing do?

A director of medical writing oversees the creation and review of scientific and regulatory documents for pharmaceutical, biotech, or healthcare companies. They manage teams of medical writers, ensure compliance with industry standards, and coordinate the development of materials such as clinical study reports, regulatory submissions, and publication content. Strong project management skills and knowledge of regulatory requirements are essential in this role.
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Director Medical Writing jobs near you
Infographic showing various Director Medical Writing job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 12% Part Time, 2% Temporary, and 10% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $263,180 per year, or $126.5 per hour.

Clinical Regulatory Writing Associate Director

Gaithersburg, MD • On-site

Ampcus Inc
IT Services • 1 - 5K employees
Learn more about Ampcus Incexternal

Other

Posted 14 days ago

Job description

Description:

Typical Accountabilities

The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company s core therapeutic areas in all phases of clinical development. Our vision is to be an industry leading organization driving strategic communication excellence to achieve successful submissions and approvals.

The Clinical Regulatory Writing Associate Director is expected to:

  • Independently manage clinical regulatory writing activities across a complex portfolio of work.
  • Author the most complex clinical-regulatory documents within a program by ensuring that relevant regulatory, technical and quality standards are achieved, and that relevant processes and best practice are applied.
  • As part of a clinical delivery or submission team, provide strategic communications leadership to projects, establish communication standards and best practice, and continuously advocate for quality and efficiency.
  • When acting as a submission lead, drive the development of the clinical Submission

Communication Strategy (cSCS).

  • Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality.
  • Drive the clinical interpretation of complex data and information and condense it into clear, concise and accurate messages that address customer information requirements.
  • Be a strategic thinker and demonstrate strategic review capabilities.
  • Proactively collaborative with other functions at the program level.
  • Support the development of Clinical Regulatory Writing Managers.
  • Drive continuous improvement and operational excellence from a communications leadership perspective, including representing the skill on drug and non-drug projects, as required

Education, Qualifications, Skills and Experience

Essential:

  • Life Sciences masters degree in an appropriate discipline.
  • Significant medical writing experience in the pharmaceutical industry or CRO.
  • Ability to advise and lead communication projects.
  • Understand drug development and communication process from development, launch through life cycle management.
  • In depth knowledge of the technical and regulatory requirements related to the role

Desirable:

  • Advanced degree in a scientific discipline (Ph.D.).
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About Ampcus

Sourced by ZipRecruiter

Ampcus Inc. is a ISO 20000, ISO 27000, ISO 9001, CMMI DEV/3 SM and CMMI SVC/3 SM certified global provider of a broad range of Technology and Business consulting services. From strategy to execution, our disciplined yet flexible approach starts and ends with our clients. By listening hard and working harder, client goals become our goals. Their success is our satisfaction. It’s why our clients sleep well at night. We believe that the success of an engagement is determined by strong project management, as well as clear communication and mutual commitment working collaboratively. Our methodology begins with listening to the customer about their needs, then working with their team to gain a clear understanding of the requirements, while providing knowledge transfer of best practices for the organization.

Industry

It services

Company size

1,001 - 5,000 Employees

Headquarters location

Chantilly, VA, US

Year founded

2004

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