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Contract Medical Writer Jobs (NOW HIRING)

AdMed Inc.

Contract Recruiter - Remote Role

We're looking for a contract / fractional recruiter to support a focused hiring period at AdMed Inc ... Competitive hourly rate Roles you'll recruit for: • Medical Writers • Account Executive • ...

Syneoshealth

OR

$95K - $210K/yr

Sr. Principal Regulatory Medical Writer - Oncology Preferred Syneos Health is a leading fully ... Further, nothing contained herein should be construed to create an employment contract.

SGS

Contract Opportunity - Medical Device Auditors

We are looking for Contract Medical Device Auditors with the following preferred experience: * Non ... Excellent communication and interpersonal, verbal, written and presentation skills * Proactive ...

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Contract Medical Writer information

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$14

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$57

How much do contract medical writer jobs pay per hour?

As of Jun 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.

How to become a freelance medical writer?

To become a freelance medical writer, develop strong writing and scientific skills, often through a background in life sciences or healthcare. Build a portfolio of writing samples, gain experience through internships or contract work, and establish a network of clients or platforms such as Upwork or Freelancer to find opportunities. Certifications like the American Medical Writers Association (AMWA) credential can enhance credibility.

How much do freelance medical writers get paid?

Freelance medical writers typically earn between $50 and $150 per hour, depending on experience, specialization, and project complexity. Rates can also vary based on the writer's expertise with regulatory writing, scientific knowledge, and the type of content produced, such as clinical study reports or marketing materials.

What is a Contract Medical Writer job?

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 in the Contract Medical Writer position, and why are they important?

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.

How much does a contract writer make?

A contract medical writer typically earns between $50,000 and $120,000 annually, depending on experience, specialization, and project scope. Contract roles often pay higher hourly rates but may lack benefits, with rates ranging from $30 to $100 per hour. Compensation varies based on expertise in medical writing, regulatory knowledge, and the complexity of assigned projects.

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 medical writers?

The demand for contract medical writers remains strong due to the ongoing need for clear, accurate scientific and clinical documentation in the healthcare and pharmaceutical industries. Medical writers with expertise in regulatory writing, clinical trial documentation, and familiarity with tools like Microsoft Word and reference management software are particularly sought after. This field offers opportunities across pharmaceutical companies, CROs, and biotech firms, often requiring certifications such as the AMWA or EMWA credentials.
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Contract Medical Writer jobs near you
Infographic showing various Contract Medical Writer job openings in the United States as of June 2026, with employment types broken down into 46% Full Time, 27% Part Time, and 27% Contract. Highlights an 64% In-person, and 36% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Medical Writer - PhD - Cardiovascular/Metabolic - Cincinnati

Medical Writer - PhD - Cardiovascular/Metabolic - Cincinnati

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, PTO

Posted 10 days ago

Key responsibilities

  • Write, edit, and maintain high-quality, complex clinical and regulatory documents, including clinical study reports, protocols, Investigator's brochures, and IND and NDA modules.

  • Coordinate and conduct quality control reviews of clinical and regulatory documents.

  • Communicate and collaborate with Sponsors and Medpace subject matter experts.

Medpace rating

8.5

Company rating: 8.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

15th of 58 rated research

Job description

Job Summary
Medpace is currently seeking candidates with a PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research for a full-time, office-based Medical Writer position. The Medical Writer will lead development of various high-quality documents critical to the development of safe and effective medical therapeutics. This is a unique opportunity that includes comprehensive training and application of the candidate's analytical skills and academic knowledge. The position includes independent work and cross-functional collaboration. If you want a rewarding position that allows you to be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!
Responsibilities
• Write, edit, and maintain high-quality, complex clinical and regulatory documents, including, but not limited to, clinical study reports, protocols, Investigator's brochures, and IND and NDA modules;
• Coordinate and conduct quality control reviews;
• Effectively communicate and collaborate with Sponsors and Medpace subject matter experts;
• Manage multiple projects and tasks simultaneously while also meeting deadlines; and
• Maintain an understanding of and compliance with company processes, and industry guidelines and regulations.
Qualifications
• PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical);
• Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience;
• Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and
• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Cincinnati Perks
  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards
  • Named a Top Workplace in 2024 by The Cincinnati Enquirer
  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Medpace logo

About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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