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Director Medical Writer Jobs (NOW HIRING)

Integrated Resources INC

medical writer

Cambridge, MA · On-site

This position works closely with the medical writing vendor and internal stakeholders within or ... Schedule 621I DIRECT # - 732-844-8724 | LinkedIn: Gold Seal JCAHO Certified for Health Care ...

Galderma

Medical Writer

Fort Worth, TX · On-site

With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact. Job Summary The Medical Writer, Medical Information is responsible ...

Real Chemistry

Medical Writer

$75K - $85K/yr

Work independently and collaboratively with medical writers and directors to develop scientifically accurate copy * Understand medical strategy and content objectives for assigned projects and ...

Costello Medical

Analyst/Medical Writer

Boston, MA · On-site

You will work closely with our Scientific Director, who is based in Boston and has more than 10 ... Medical Communications - Medical Writer Medical Communications at Costello Medical encompasses both ...

MSS MJH Shared Services

Medical Writer

Charleston, WV

$85K - $100K/yr

The Medical Writer plays a critical role in creating accurate, engaging, and compliant scientific ... You'll work closely with scientific directors, editors, designers, and subject matter experts to ...

MJH Life Sciences

Medical Writer

Cranbury, NJ · On-site

$85K - $100K/yr

The Medical Writer plays a critical role in creating accurate, engaging, and compliant scientific ... You'll work closely with scientific directors, editors, designers, and subject matter experts to ...

Kura Oncology

The Senior Director, Medical & Regulatory Writing serves as subject matter expert on clinical ... medical writer in a pharmaceutical, biotech, or CRO environment. Oncology experience preferred.

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 ...

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How much do director medical writer jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for director medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director Medical Writer, and why are they important?

To thrive as a Director Medical Writer, you need advanced expertise in medical writing, a deep understanding of clinical research, and usually a graduate degree in life sciences or a related field. Familiarity with regulatory submission standards, document management systems, and tools like EndNote or electronic common technical document (eCTD) software is typically required. Exceptional leadership, project management, and communication skills distinguish top performers in this position. These competencies are crucial for ensuring the production of accurate, compliant documents that meet tight deadlines and regulatory expectations.

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 medical writers or directors often have higher compensation, with salaries ranging from mid to high six figures in some regions, especially when combined with specialized skills and certifications. The profession generally offers stable income, especially in pharmaceutical, biotech, and healthcare industries where clear communication and regulatory knowledge are valued.

What are the main challenges a Director Medical Writer faces when managing multiple writing projects across different therapeutic areas?

A Director Medical Writer often oversees a diverse portfolio of projects, each with its own timelines, regulatory requirements, and subject matter experts. Balancing these responsibilities requires strong project management skills, as well as the ability to quickly adapt to new therapeutic areas and evolving client expectations. Clear communication and collaboration with cross-functional teams, including regulatory affairs, clinical operations, and external stakeholders, are essential to ensure accuracy and compliance. Staying current with industry standards and mentoring junior writers can also present additional challenges, but these efforts contribute to overall team success and professional growth.

What does a director of medical writing do?

A director of medical writing oversees the creation and review of scientific and regulatory documents such as clinical study reports, protocols, and regulatory submissions. They manage teams of medical writers, ensure compliance with industry standards, and coordinate with cross-functional teams to deliver accurate, clear, and timely documentation for healthcare and pharmaceutical industries.

Is there a demand for medical writers?

The demand for medical writers is strong due to the growing need for clear scientific communication in healthcare, pharmaceuticals, and regulatory industries. Medical writers with expertise in clinical research, regulatory writing, and familiarity with tools like ICH guidelines are highly sought after, with job opportunities available in both full-time and freelance roles.

What is the highest salary for a medical writer?

The highest salary for a medical writer can exceed $150,000 annually, especially for senior or specialized roles in pharmaceutical or biotech companies. Factors such as experience, certifications, and the complexity of the projects influence compensation levels.

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

AspectDirector Medical WriterMedical Writer
CredentialsTypically requires advanced degrees (MD, PhD, PharmD) and extensive experienceUsually holds a Bachelor's, Master's, or PhD in life sciences or related fields
Work EnvironmentLeads teams, manages projects, and interacts with senior stakeholdersFocuses on writing and editing scientific documents under supervision
Industry UsageUsed in pharmaceutical, biotech, and healthcare companies for strategic document oversightCommonly employed in similar industries for document creation and review

The main difference between a Director Medical Writer and a Medical Writer lies in their level of responsibility and experience. Directors oversee teams, manage projects, and contribute to strategic decisions, while Medical Writers primarily focus on producing and editing scientific documents. Both roles require strong scientific credentials, but the Director position demands more leadership and management skills.

What does a Director Medical Writer do?

A Director Medical Writer leads a team of medical writers responsible for creating scientific documents such as clinical study reports, regulatory submissions, and publications. They oversee the quality and accuracy of all written materials, ensuring compliance with regulatory standards and guidelines. Additionally, they collaborate with cross-functional teams, provide strategic guidance, and mentor junior writers within the organization. Their role is critical in translating complex clinical data into clear, concise content for regulatory agencies and healthcare professionals.
What cities are hiring for Director Medical Writer jobs? Cities with the most Director Medical Writer job openings:
What are the most commonly searched types of Medical Writer jobs? The most popular types of Medical Writer jobs are:
What states have the most Director Medical Writer jobs? States with the most job openings for Director Medical Writer jobs include:
Director Medical Writer jobs near you
Infographic showing various Director Medical Writer job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 40% Full Time, 58% Part Time, and 1% Temporary. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Associate Director Medical Writing

Meet Life Sciences

Santa Clara, CA • Hybrid

Other

Posted 17 days ago

Job description

Associate Director, Medical Writing (Hybrid - SF Bay Area)


We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory documents in support of complex drug development programs. This individual will play a key role in shaping document strategy, ensuring scientific accuracy, and driving cross-functional alignment across clinical, regulatory, and biostatistics teams.


This is a hybrid role based in the San Francisco Bay Area. Relocation package is available.


Key Responsibilities

  • Lead the planning, authoring, and review of clinical and regulatory documents, including clinical study reports (CSRs), protocols, investigator brochures (IBs), and submission documents
  • Serve as the medical writing lead on complex, multi-phase programs, including late-stage development and regulatory submissions
  • Collaborate cross-functionally with Clinical Development, Regulatory Affairs, Biostatistics, and Clinical Operations to ensure aligned messaging and data interpretation
  • Drive document strategy and timelines to support IND, NDA, and other global regulatory submissions
  • Ensure all documents meet regulatory requirements, internal standards, and industry best practices
  • Manage external medical writers and vendors as needed
  • Provide mentorship and guidance to junior writers and cross-functional team members
  • Contribute to process improvements and development of templates, style guides, and best practices


Qualifications

  • PhD (or equivalent advanced degree) in life sciences, pharmacy, or a related field required
  • 8+ years of medical writing experience within biotech, pharma, or CRO environments
  • Demonstrated experience supporting complex clinical development programs and regulatory submissions (IND, NDA, BLA, etc.)
  • Strong expertise in authoring clinical and regulatory documents (e.g., CSRs, protocols, IBs)
  • Proven ability to manage multiple writing projects and timelines in a fast-paced environment
  • Excellent written and verbal communication skills, with strong attention to detail
  • Experience working in cross-functional teams and influencing without direct authority
  • Prior leadership or mentoring experience preferred


If this role sounds of interest, please reach out to tanya.kochan@meetlifesciences.com.

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