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Consultant Medical Writer Jobs (NOW HIRING)

Principal Medical Writer

$172K - $232K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... consultants, contractors and vendors. * Collaborate effectively with Biometrics, Clinical ... support the medical writing needs of a growing organization and assist in training staff and ...

Medical Writer IV

Abbott, TX · On-site +1

$65 - $71/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic ... Consultants Eligible Benefits Upon Waiting Period: * Medical and Prescription Drug Plans * Dental ...

New

$120 - $180/hr

Beyond managing the consultant program day to day, you\'ll partner with our product team to give feedback on our internal AI tooling and help shape how we deliver medical writing services going ...

Showing results 21-40

Consultant Medical Writer information

See salary details

$11

$46

$78

How much do consultant medical writer jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for consultant medical writer in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

How does a consultant medical writer typically collaborate with clients and subject matter experts during a project?

As a Consultant Medical Writer, effective collaboration with clients and subject matter experts (SMEs) is essential for producing accurate and high-quality documents. You will frequently coordinate with clinical researchers, regulatory teams, and healthcare professionals to gather technical information, clarify data, and ensure compliance with industry standards. Communication is often managed through virtual meetings, email correspondence, and document review cycles, requiring strong interpersonal and project management skills. Building positive relationships with stakeholders helps streamline feedback and ensures the final deliverables meet both scientific and regulatory expectations.

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

AspectConsultant Medical WriterMedical Writer
CredentialsTypically requires a life sciences degree, advanced degree preferred, and relevant certificationsUsually holds a degree in life sciences, with or without additional certifications
Work EnvironmentOften works as a freelancer or contractor, collaborating with multiple clientsTypically employed by pharmaceutical or biotech companies, agencies, or CROs
Industry UsageCommonly used in consulting, freelance projects, and contract rolesWidely used within pharmaceutical, biotech, and healthcare industries

In summary, Consultant Medical Writers often work independently or as contractors, focusing on project-based work across various clients, while Medical Writers are usually employed full-time within organizations. Both roles require strong scientific knowledge and writing skills, but their work settings and employment types differ.

What are the key skills and qualifications needed to thrive as a consultant medical writer?

To thrive as a Consultant Medical Writer, you need a strong background in life sciences or medicine, excellent writing skills, and typically an advanced degree such as a PhD or PharmD. Familiarity with referencing software (e.g., EndNote), regulatory documentation systems, and guidelines like ICH or GPP3 is often required. Attention to detail, project management abilities, and clear communication help distinguish top performers in this field. These skills are vital for producing accurate, compliant, and impactful medical documents that support research, regulatory submissions, and scientific communication.

What is a consultant medical writer?

A Consultant Medical Writer is a professional who provides expert writing and editing services for medical and scientific documents, often on a freelance or contract basis. They typically work with pharmaceutical companies, research organizations, or healthcare communications agencies to develop materials such as clinical study reports, regulatory submissions, journal articles, and educational content. Their expertise combines scientific knowledge with strong communication skills to ensure complex medical information is accurately and clearly presented. Consultant Medical Writers may also advise clients on regulatory requirements and publication strategies. This role requires advanced degrees in life sciences or medicine and experience in medical writing.
More about Consultant Medical Writer jobs
Infographic showing various Consultant Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

$172K - $232K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago


Job description

The Principal Medical Writer (equivalent to Associate Director) represents medical writing on multi-disciplinary teams, collaborates on the development of clinical documents in accordance with all applicable regulations, Good Clinical Practices, and Standard Operating Procedures (SOPs), and oversees the work of contract writers on the clinical program as well as other writers who may work on the program.
Responsibilities:
  • Produce high-quality and on-time clinical documents
  • Independently plan, coordinate, develop, update, and revise key documents, including clinical protocols, investigator brochures, clinical study reports, integrated efficacy and safety summaries, and related documents. Other documents may include informed consent forms, health authority briefing books, and scientific publications.
  • Independently lead supplemental filings, Type 2 Variations, rest-of-world filings, and clinical responses to questions
  • Provide medical writing subject matter expertise and leadership to project teams and collaborate with the Medical Writing line management to ensure proper planning and resourcing for upcoming project team writing deliverables.
  • Facilitate/manage efficient review and finalization process for documents produced internally and/or externally by consultants, contractors and vendors.
  • Collaborate effectively with Biometrics, Clinical Operations, Clinical Development, Pre-Clinical Development, Program Management, Research, Quality, and Corporate Communications, as well as with external stakeholders.
  • Contribute to the development and standardization of templates and related processes to support the medical writing needs of a growing organization and assist in training staff and contractors on MW processes.
  • Assist the line managers in the training and development of junior staff.

Qualifications:
  • Bachelor's degree in Life Science with relevant writing expertise or in English/Communications with relevant science expertise. Advanced degree and/or professional certification/credentials preferred.
  • 7+ years of experience as a medical writer in the sponsor/CRO setting. Experience with regulatory submissions (NDA/BLA/MAA) strongly preferred. CTA/IND experience is a plus.
  • Some experience with developing MW processes and standards preferred
  • In-depth knowledge of Good Clinical Practices, FDA regulations, ICH guidelines, and the drug development process.
  • Successful track record of managing multiple projects in a fast-paced and deadline-driven environment.
  • Knowledge of eCTD formatting and EDMS systems preferred.
  • Experience overseeing the work of contract writers.
  • Impeccable attention to detail.
  • Must be proficient with Microsoft Windows, Word, Excel, and PowerPoint.
  • Demonstrate clear alignment with Alnylam Core Values including,

    • Commitment to People
    • Innovation and Discovery
    • Purposeful Urgency
    • Open Culture
    • Passion for Excellence

U.S. Pay Range
$172,000.00 - $232,800.00
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers
About Alnylam
We are the leader in RNAi therapeutics - a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.