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Director Medical Writing Jobs in Washington (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

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Director Medical Writing information

See Washington salary details

$14.7K

$263.2K

$404.3K

How much do director medical writing jobs pay per year?

As of Sep 4, 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.

What are the most commonly searched types of Medical Writing jobs in Washington?

The most popular types of Medical Writing jobs in Washington are:

What are popular job titles related to Director Medical Writing jobs in Washington?

For Director Medical Writing jobs in Washington, the most frequently searched job titles are:

What cities in Washington are hiring for Director Medical Writing jobs?

Cities in Washington with the most Director Medical Writing job openings:

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.

Manager/Associate Director of Regulatory Medical Writing

DaMar Staffing

Washington, DC • On-site

$95 - $176/hr

Other

Medical, Retirement, PTO

Posted 5 days ago


Key responsibilities

  • Manage project-specific tasks for medical writing staff, including overseeing recruitment, performance appraisals, and professional development.

  • Review and edit departmental outputs to ensure they meet quality standards for completeness and accuracy.

  • Support the medical writing leadership team in strategizing document development, preparing budgets and timelines, and participating in medical writing deliverables.


Job description

Join Syneos Health as a Manager/Associate Director of Regulatory Medical Writing

Syneos Health is at the forefront of biopharmaceutical solutions, dedicated to accelerating client success. We bring unique insights from clinical, medical affairs, and commercial sectors to tackle contemporary market challenges. Our Clinical Development framework places the customer and patient at the core of our operations. We are continuously seeking innovative ways to streamline our processes, not only making Syneos Health easier to collaborate with but also a more fulfilling place to work. Be part of a passionate team dedicated to transforming lives and delivering therapies efficiently. Explore the impact of our 29,000 employees across 110 countries.

Your Role and Responsibilities
  • Manage project-specific tasks for medical writing staff, including overseeing salary administration, recruitment, performance appraisals, and professional development.
  • Review and edit departmental outputs to ensure they meet quality standards for completeness and accuracy.
  • Maintain adherence to Sponsor objectives while ensuring high-quality standards are met.
  • Support the medical writing leadership team in strategizing document development and presenting quarterly business updates.
  • Assist with preparing budgets and timelines for medical writing activities related to clinical development projects.
  • Facilitate project metrics tracking and contribute to departmental performance metrics.
  • Support business development efforts by assisting with proposal development and customer meetings.
  • Develop productive relationships with internal and external customers and lead cross-functional teams.
  • Review the performance of medical writing team members and provide guidance as necessary.
  • Create and maintain departmental Standard Operating Procedures (SOPs) and templates.
  • Participate in the planning and writing of medical writing deliverables when required.
  • Conduct senior reviews of medical writing outputs, as well as reviews of statistical analysis plans and related documents.
  • Undertake additional relevant duties as assigned, with potential travel required (up to 25%).

At Syneos Health, we are committed to fostering an environment where our people can thrive and develop. We offer valuable benefits including health coverage, a 401k match, employee stock purchase eligibility, performance bonuses, and flexible paid time off.

Salary Range: $95,000.00 - $175,700.00

Please note that actual salary will depend on qualifications, skills, and experience.

Discover Syneos Health. In the past five years, we have partnered with 94% of all novel FDA-approved drugs and 95% of EMA authorized products. We have contributed to over 200 studies globally.

No matter your role, you are encouraged to drive initiative and innovation in a competitive landscape. Join us and shape the future at Syneos Health.

Tasks and responsibilities may evolve as required or as deemed necessary by the company. The description does not constitute a contractual obligation.

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