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Contract Medical Writing Jobs (NOW HIRING)

Dexian

Medical Writer, US Medical Affairs

Whippany, NJ · On-site

$45 - $51/hr

... medical writing and administration of research, partnerships, and HCPs (healthcare providers) contracts. Reporting to the Head of Medical Affairs for the Americas, the Medical Writer will be ...

Veristat

Minimum of 7 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. * Experience as a lead writer on a minimum of 20 manuscripts, 20 ...

OSI Pharmaceuticals

Senior Medical Writer

Boulder, CO · On-site

Manages work of contract writers. Develops SOPs and templates for the CTD, protocols, final reports ... related medical writing experience. Outstanding writing, analytical and research skills a must.

Chenega Corporation

Physician

Rockville, MD · Remote

$150/hr

Serve as a Contract Medical Reviewer (CMR) who writes medical eligibility determination recommendations via a medical report in alignment with the Government provided training and instruction. * The ...

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How much do contract medical writing jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for contract medical writing 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.

What types of documents do contract medical writers typically work on, and how does the workflow usually look?

Contract medical writers commonly create regulatory submissions (such as clinical study protocols, investigator brochures, and clinical study reports), medical publications, and educational materials for healthcare professionals or regulatory authorities. The workflow usually begins with a project briefing, followed by extensive literature review, drafting, and rounds of review with subject matter experts, regulatory affairs, or clients. Most projects require frequent communication via email or virtual meetings and adherence to strict deadlines. Contract medical writers often work independently but must be flexible and responsive to feedback and changing priorities, which makes time management and adaptability crucial for success.

Is there a demand for medical writers?

There is a strong and growing demand for medical writers due to the increasing need for clear scientific communication in healthcare, pharmaceuticals, and regulatory industries. Medical writers with expertise in clinical research, regulatory writing, and familiarity with tools like document management systems are especially sought after across various organizations.

How much does a freelance medical writer make?

Freelance medical writers typically earn between $50 and $150 per hour, depending on experience, specialization, and project complexity. Many also charge per project, with rates varying based on the scope and length of the work, and successful freelancers often have strong scientific backgrounds and writing skills to command higher fees.

How to get into freelance medical writing?

To start as a freelance medical writer, build expertise in a medical or scientific field, develop strong writing skills, and create a professional portfolio. Gaining experience through internships, certifications like the AMWA Medical Writer Certification, and networking on platforms such as LinkedIn can help establish credibility and attract clients.

What is a Contract Medical Writing job?

A Contract Medical Writing job involves creating regulatory, clinical, or scientific documents for pharmaceutical, biotech, or medical device companies on a contract or freelance basis. Medical writers in these roles develop documents such as clinical study reports, regulatory submissions, or scientific publications. They work independently or through agencies, often collaborating with researchers, clinicians, and regulatory teams. These roles offer flexibility in workload and project selection while requiring strong scientific knowledge and writing expertise.

Are medical writers going to be replaced by AI?

Medical writers play a crucial role in creating accurate, compliant, and complex scientific documents, which currently require human expertise and critical thinking that AI cannot fully replicate. While AI tools can assist with drafting and data analysis, the nuanced understanding of medical content, regulatory requirements, and audience needs ensures that human medical writers remain essential in the field.

What are the key skills and qualifications needed to thrive in the Contract Medical Writing position, and why are they important?

To thrive as a Contract Medical Writer, you need a strong background in life sciences or pharmacy, excellent written communication skills, and experience with scientific or regulatory documentation. Familiarity with tools such as Microsoft Office Suite, reference management software, and guidelines like ICH, GCP, or AMA style, as well as relevant certifications (e.g., AMWA), is highly beneficial. Outstanding organization, time management, and the ability to communicate complex information clearly with diverse stakeholders will set you apart. These abilities ensure the creation of accurate, compliant medical documents and support effective collaboration in fast-paced, deadline-driven environments.

More about Contract Medical Writing jobs
What cities are hiring for Contract Medical Writing jobs? Cities with the most Contract Medical Writing job openings:
What are the most commonly searched types of Medical Writing jobs? The most popular types of Medical Writing jobs are:
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What job categories do people searching Contract Medical Writing jobs look for? The top searched job categories for Contract Medical Writing jobs are:
Contract Medical Writing jobs near you
Infographic showing various Contract Medical Writing job openings in the United States as of July 2026, with employment types broken down into 57% Full Time, 22% Part Time, 1% Temporary, and 20% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Senior Medical Writer (Fixed-Term Contract)

Compass Pathways

New York, NY • On-site

$135K - $185K/yr

Full-time, Contractor

Posted 6 days ago

Job description

Company introduction:
Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. The Company is headquartered in London, UK, with offices in New York City in the US. We focus on developing novel treatments that have the potential to improve the lives of those who are suffering with mental health conditions and who are not helped by current treatments.
We are pioneering a new paradigm for treating mental health conditions focused on rapid and durable responses through the development of our investigational COMP360 synthetic psilocybin treatment, potentially a first in class treatment. COMP360 has Breakthrough Therapy designation from the US Food and Drug Administration (FDA) and has received Innovative Licensing and Access Pathway (ILAP) designation in the UK for treatment-resistant depression (TRD) due to the pressing unmet need in this area.
We are currently in phase 3 for TRD, have completed phase 2 studies for both post-traumatic stress disorder (PTSD) and anorexia nervosa and are planning a further late-stage study in PTSD. We envision a world where mental health means not just the absence of illness but the ability to thrive. - Compass Pathways.
Job overview:
The Senior Medical Writer is responsible for developing various clinical regulatory documents related to our investigational product, our proprietary psilocybin therapy. This role leads document preparation, ensures adherence to regulatory and company standards, coordinates outsourced writing services, and collaborates with multidisciplinary teams to support the regulatory sciences function.
Location: Hybrid in our New York City office or remote on the east coast in the United States.
Reports to: Director, Medical Writing.
Duration: 6-month contract.
Roles and responsibilities
(Include but are not limited to):
  • Prepares and co-ordinates responses to regulatory agency information requests
  • Leads preparation of clinical regulatory documents, including CSRs, protocols, IB and clinical summaries (Module 2.7.x and ISE/ISS)
  • Ensures Compass clinical documents are clear, accurate, and written in accordance with the relevant guidance and best practice
  • Oversees and co-ordinates outsourced medical writing services as required
  • Provides subject matter expertise as a member of the regulatory sciences team
  • Accountable for compliance with ethical and scientific standards, regulatory requirements, and the Compass Quality Management System; ensuring participant safety, data integrity and accuracy throughout the trial process

Candidate profile:
  • Minimally a Bachelor's degree in the life or health sciences; MSc or PhD preferred
  • Experience in supporting regulatory submissions as a writer within the pharmaceutical industry/CRO
  • Experience in leading the development of clinical documents as part of a multi-functional team, including CSRs, IBs, clinical summaries, ISS/ISE
  • Broad working knowledge of the clinical drug development process with experience of integrating information into clinical regulatory documents
  • Knowledge of relevant ICH guidance relating to clinical regulatory documentation
  • Excellent written English with aptitude for clear and concise writing
  • Excellent attention to detail and editorial skills
  • Flexibility in adapting to changing circumstances or new information
  • Alignment to our company culture and values

[For NYC]Compensation Description (annually):
Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.
Base pay is one part of the Total Package that is provided to compensate and recognise employees for their work and any role at Compass, regardless of the location, is eligible for additional discretionary bonuses and equity.
[Base salary per annum]:
$135,000-$185,000 USD
Benefits & Compensation:
For an overview of our benefits package and compensation information, please visit "Working at Compass".
Equal opportunities:
Reasonable accommodationWe are committed to building a workplace where everyone's wellbeing matters. If you need reasonable accommodation during the interview process to be at your best, please let our recruiting team know.
UK applicants
We are proud of our commitment to diversity and equality (pursuant to the Equality Act 2010). We do not discriminate based upon race, religion or belief, colour, nationality, ethnic or national origin, gender, pregnancy or maternity, marital or civil partner status, sexual orientation, gender reassignment, age or disability.
US applicants
Compass Pathways is proud to be an equal opportunity employer. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, and related medical conditions), ethnicity, age, disability, sexual orientation, gender identity, gender expression, military service, genetic information, familial or marital status, or any other status, category, or characteristic protected by applicable law.
Sponsorship:
Unfortunately, we cannot sponsor employment visas and can only accept applications if you have employment rights in the country to which you are applying.
Data Privacy:
All data is confidential and protected by all legal and data privacy requirements, please see our recruitment Privacy Notice to learn more about how we process personal data.

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