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Contract Medical Writer Jobs (NOW HIRING)

Revolution Medicines

Principal Medical Writer

Mentors junior and contract medical writers on both document and timeline management. Required Skills, Experience and Education: * 8-11 years of clinical regulatory writing experience within one or ...

Revolution Medicines

Principal Medical Writer

$211K - $264K/yr

Mentors junior and contract medical writers on both document and timeline management. Required Skills, Experience and Education: * 8-11 years of clinical regulatory writing experience within one or ...

Trident Consulting

Medical Writer

Irvine, CA · On-site

$40 - $44/hr

Contract (W2) Pay Rate: $40/hr - $44/hr on W2 Duration: 6 Months About the Role We are seeking a Medical Writer II to support clinical and regulatory documentation activities for current and pipeline ...

Clear Point Consultants

Medical Writer

Boston, MA · On-site

$55 - $70/hr

Medical Writing Science Manager 📍 Boston, MA | Hybrid -- 3 days onsite / 2 days remote 💼 Initial 2-month contract | Potential for extension or conversion 💰 $55-$70/hour ⏰ 40 hours/week We ...

Biodesix, Inc.

Medical Writer

$90K - $130K/yr

Minimum 3 years of medical writing experience within biotechnology, diagnostics, pharmaceuticals, contract research organizations, medical communications agencies, or related healthcare environments.

Veristat

Principal Medical Writer

England, AR · On-site +1

Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Veristat

Principal Medical Writer

Ontario, CA · On-site +1

Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Veristat

Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Veristat

Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Veristat

Principal Medical Writer

Scotland, PA · On-site +1

Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Veristat

Principal Medical Writer

Columbia, SC · On-site +1

Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Veristat

Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Alnylam Pharmaceuticals

Principal Medical Writer

$172K - $232K/yr

The Principal Medical Writ er (equivalent to Associate Director) represents medical writing on ... Experience overseeing the work of contract writers. * Impeccable attention to detail. * Must be ...

Integrated Resources INC

Medical Writer - I

Raynham, MA · On-site

This is Contract position with my direct client Overview: The Medical Writer Specialist is responsible for preparation of documents that support the presentation and/or publication needs of assigned ...

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Contract Medical Writer information

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How much do contract medical writer jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for contract 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 is a contract medical writer?

A Contract Medical Writer is a professional who creates scientific documents on a freelance or contract basis for pharmaceutical, biotech, or healthcare companies. They develop clinical study reports, regulatory submissions, manuscripts, and other medical content. Unlike full-time employees, contract medical writers work on a project-by-project basis, often remotely. They must have strong writing skills, scientific knowledge, and an understanding of medical regulations. This role offers flexibility but requires self-discipline and deadline management.

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

To thrive as a Contract Medical Writer, you need a thorough understanding of scientific concepts, excellent writing skills, and often an advanced degree in life sciences or a related field. Familiarity with regulatory documentation formats (such as ICH, FDA, or EMA standards), medical journal requirements, and tools like Microsoft Office Suite or referencing software is vital. Strong organizational skills, attention to detail, and the ability to communicate complex information clearly are essential soft skills. These capabilities ensure accuracy, compliance, and the effective communication of scientific data to diverse audiences in the healthcare industry.

What types of projects can I expect to work on as a contract medical writer?

As a Contract Medical Writer, you may work on a variety of projects including clinical trial protocols, regulatory submissions, scientific manuscripts, patient education materials, and medical communications for conferences or publications. The work is typically project-based, with deadlines and deliverables defined by clients or pharmaceutical companies. You will often collaborate remotely with clinical researchers, regulatory teams, and subject matter experts to gather information and ensure accuracy. This diversity of projects keeps the role dynamic and allows for continuous learning in different therapeutic areas or document types.

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Contract Medical Writer jobs near you
Infographic showing various Contract Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Medical Writer

Three Point Solutions, Inc.

Maple Grove, MN • On-site

Full-time

Re-posted 28 days ago

Job description

Job Title: Medical Writer
Client: Medical Device Manufacturing Company
Duration: 12 Months
Location: Maple Grove, MN, 55311
**Mandatory- Must be US Citizen or Green Card Holder Only
Key Words:
  • CER (Clinical Evaluation Review/Report) Writing
  • MDR (Medical Device Regulations)
  • EU (European Union)
  • Literature Review (e.g., PubMed)

Responsibilities:
  • Write and review scientific manuscripts, congress abstracts, and scientific meeting presentations aligned with journal and congress guidelines.
  • Prepare clinical content for study investigator meetings, interim data analyses, and other internal/external meetings related to clinical studies.
  • Create symposia (non-CME), speaker decks, post-meeting slide decks, topical slide decks, and other Professional Education modules as needed.
  • Collaborate extensively with internal medical leadership, clinical research scientists, clinical trial managers, medical affairs managers, statisticians, and other medical writers as part of publication teams.
  • Develop partnerships with study investigators, external authors, and interact externally with journals, conference organizers, and freelance/contract medical writers.
  • Ensure clinical data is represented accurately in published literature, slide sets, and other materials.
  • Lead and organize document production meetings and related activities.
  • Review documents related to clinical evidence for proper evaluation and presentation of data, methodology, and interpretation.

Required Qualifications:
  • Degree in Life Sciences (Advanced degree preferred).
  • Experience in Medical Device or Pharmaceutical Industry with a focus on Medical Writing or Clinical Research.
  • Extensive experience in writing, editing, and submitting publications to journals and congresses.

Preferred Qualifications:
  • 5-7 years of relevant experience.
  • Therapeutic area knowledge in peripheral interventions is desired.
  • Excellent written, analytical, verbal, and communication skills.
  • Ability to manage multiple projects independently and meet deliverables on time.
  • Capable of working effectively in a matrix environment.
  • Ability to develop strategic solutions to significant business issues.
  • Commitment to patient safety and product quality by adhering to the Quality Policy and documented quality processes and procedures.

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