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Contract Medical Writer Jobs (NOW HIRING)

Revolution Medicines

Principal Medical Writer

$201K - $251K/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 ...

Integrated Resources INC

Medical Writer

Cambridge, MA · On-site

Coordinates medical writing support for programs with internal and contract writers. Additionally, must posess the ability to guide and assists medical writers in the writing of documents that are ...

Medasource

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

Lead Medical Writer Remote (must be based in EST) Compensation: $80-$90 per hour Contract Length: 2 month Contract to Hire (40 hours/week) Start Date: 7/1/26 ABOUT THE ROLE Our client is a global ...

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

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 ...

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

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

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

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 ...

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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 9, 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.

Do medical writers make good money?

Contract medical writers typically earn competitive salaries that vary based on experience, specialization, and location. They often work on a project basis or hourly rates, with experienced writers and those with specialized knowledge earning higher compensation. The role requires strong writing skills, scientific understanding, and familiarity with regulatory guidelines.

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.

How to become a contract medical writer?

To become a contract medical writer, typically a bachelor's degree in life sciences, pharmacy, or related fields is required, along with strong writing skills and knowledge of medical terminology. Gaining experience through internships, freelance projects, or entry-level roles helps build a portfolio. Familiarity with regulatory guidelines and tools like Microsoft Word or reference management software is also beneficial.

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.

Is there a demand for contract medical writers?

Yes, there is consistent demand for contract medical writers due to the ongoing need for clear, accurate scientific and clinical documentation in the pharmaceutical, biotech, and healthcare industries. These roles often require strong writing skills, knowledge of regulatory guidelines, and familiarity with tools like Microsoft Word and reference management software. The demand is driven by the need for specialized content such as clinical study reports, regulatory submissions, and medical communications.
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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, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% 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 7 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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