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Remote Contract Medical Writer Jobs (NOW HIRING)

GlaxoSmithKline

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

Olema Oncology

Lead Senior Medical Writer

Boston, MA · On-site +1

$160K - $175K/yr

About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...

Olema Oncology

Lead Senior Medical Writer

San Francisco, CA · On-site +1

$160K - $175K/yr

About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...

Trilogy

Senior/Principal Medical Writer - USA

Durham, NC · On-site +1

$120K - $159K/yr

... remote) from our Durham, NC, USA office. You willbe responsible for: * Preparinga variety of ... As a Senior/Principal Medical Writer, you will: * Function as a lead writer to prepare a variety of ...

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Remote Contract Medical Writer information

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How much do remote contract medical writer jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for remote 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 the difference between Remote Contract Medical Writer vs Remote Full-Time Medical Writer?

AspectRemote Contract Medical WriterRemote Full-Time Medical Writer
CredentialsTypically requires medical or scientific degrees, writing experience, and industry certificationsSame as contract; often requires similar credentials and certifications
Work EnvironmentProject-based, flexible hours, short-term engagementsPermanent employment, consistent schedule, ongoing projects
Employer & Industry UsageFreelance or consulting firms, biotech, pharma companiesPharmaceutical companies, CROs, biotech firms
Search & Comparison IntentHigh overlap in skills, project scope, and industry contextSimilar roles with different employment types

The main difference between a Remote Contract Medical Writer and a Remote Full-Time Medical Writer lies in employment type and engagement duration. Contract writers work on specific projects with flexible hours, while full-time writers have ongoing employment with consistent schedules. Both roles require similar credentials and industry experience, making them comparable in skills and responsibilities.

What is a Remote Contract Medical Writer?

A Remote Contract Medical Writer is a professional who creates scientific documents, such as clinical study reports, regulatory submissions, or educational materials, for pharmaceutical, biotech, or healthcare organizations while working remotely on a contract basis. They translate complex medical data into clear, accurate, and compliant content tailored to the target audience, such as regulatory agencies, healthcare providers, or patients. These writers typically collaborate with subject matter experts, researchers, and regulatory teams, and their work often follows strict industry guidelines and deadlines. Remote contract roles offer flexibility and the ability to work with multiple clients from different locations.

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

To thrive as a Remote Contract Medical Writer, you need a strong background in life sciences, excellent research abilities, and proven writing skills, often supported by a relevant degree or advanced certification. Familiarity with regulatory documentation, referencing software (such as EndNote), and platforms like Microsoft Office or document management systems is typically required. Keen attention to detail, time management, and clear communication are essential soft skills for meeting deadlines and collaborating remotely. These skills ensure the creation of accurate, compliant, and high-quality medical documents for clients and regulatory agencies.

What are some common challenges faced by remote contract medical writers, and how can they be managed?

Remote contract medical writers often encounter challenges such as managing multiple deadlines for different clients, adapting to varying writing styles and guidelines, and maintaining clear communication across virtual teams. To address these, it’s important to develop strong organizational skills, set clear expectations with clients, and utilize project management tools. Regular check-ins and proactive communication with clients and collaborators help ensure alignment and smooth workflow.
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What cities are hiring for Remote Contract Medical Writer jobs? Cities with the most Remote Contract Medical Writer job openings:
What are the most commonly searched types of Remote Medical Writer jobs? The most popular types of Remote Medical Writer jobs are:
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Remote Contract Medical Writer jobs near you
Infographic showing various Remote Contract Medical Writer job openings in the United States as of June 2026, with employment types broken down into 99% Full Time, and 1% Contract. Highlights an 37% Physical, 3% Hybrid, and 60% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Senior Medical Writer - Medical Information

Senior Medical Writer - Medical Information

Thermo Fisher Scientific

NC • Remote

Full-time

Posted 9 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 408 frontline employees who took The Breakroom Quiz

190th of 527 rated manufacturers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation

The Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. The Senior Medical Writer may assist program manager. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
What You'll Do:

  • Serve as a primary writer who creates and provides input on routine deliverables, such as medical information documents, publications and clinical study documents.

  • Develop complex medical and scientific documents, including AMCP dossiers, infographics, slide presentations, manuscripts, study documents for complex programs.

  • Review documents prepared by team members. May provide training and mentorship for medical writers and new hires.

  • Ensure compliance with applicable SOPs, WI, quality processes, and requirements for documents. Provide input on and independently develop best practices for achieving optimal results, including various client-specific processes.

  • May function as a project lead or assist with program management activities. Duties could include developing timelines, budgets, forecasts, and contract modifications; tracking deliverable metrics; and representing medical writing team in client meetings.  


Education & Experience Requirements:

  • PharmD

  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).

  • Experience working in the pharmaceutical/CRO industry preferred

  • Additional qualifications in medical writing or medical information advantageous


Knowledge, Skills, Abilities:

  • Excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills

  • Ability to interpret and present complex data accurately and concisely

  • Ability to work on own initiative and effectively within a team

  • Excellent administration, attention to detail, organizational, planning, and problem-solving skills

  • Strong project management skills

  • Excellent oral and written communication skills with strong presentation skills

  • Significant knowledge of global, regional, national and other document development guidelines

  • Great judgment and decision-making skills; strong negotiation skills

  • Excellent computer skills and skilled with client templates; good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook)

Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.

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