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Contract Medical Writing Jobs (NOW HIRING)

TechData Service Company LLC

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Medical Writer (Remote)

OR · Remote

$85 - $90/hr

Medical Writer Contract Position - 6 months with potential extension Position Summary Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in ...

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 ...

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.

Medasource

HEOR Medical Writer

Whippany, NJ · On-site +1

$30 - $40/hr

Remote Duration: 6 month contract with the potential for extension, based on performance Targeted ... The position requires strong scientific and HEOR literacy, excellent writing skills, and the ...

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 ...

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 Writing information

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$11

$46

$78

How much do contract medical writing jobs pay per hour?

As of Jun 30, 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.

How much does a contract writer make?

Contract medical writers typically earn between $50 and $150 per hour, depending on experience, specialization, and project complexity. Freelance rates can vary widely, with some writers charging higher rates for specialized knowledge or regulatory expertise.

Is there a demand for medical writers?

There is strong demand for medical writers across pharmaceutical, biotech, and healthcare industries due to ongoing regulatory requirements and the need for clear scientific communication. Skilled medical writers with knowledge of clinical trials, regulatory guidelines, and proficiency in tools like Microsoft Word and reference management software are especially sought after.

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 familiarity with industry guidelines, such as ICH E6 or CONSORT, and obtaining relevant certifications can enhance credibility. Networking through professional associations and platforms like Upwork or Freelancer can help secure initial 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.

Will medical writing jobs be replaced by AI?

Medical writing jobs involve complex interpretation of scientific data, regulatory knowledge, and clear communication, which currently cannot be fully replaced by AI. While AI tools can assist with data analysis and drafting, human expertise remains essential for accuracy, compliance, and nuanced understanding in medical writing roles.

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:
What states have the most Contract Medical Writing jobs? States with the most job openings for Contract Medical Writing jobs include:
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 June 2026, with employment types broken down into 27% Full Time, 49% Part Time, and 24% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Sr. Director, Global Head of Medical Writing/CTT

Merck Group

Billerica, MA • On-site

$234K - $352K/yr

Full-time

Medical, Retirement, PTO

Posted 6 days ago

Job description

Work Location: Billerica, Massachusetts
Shift: No
Department: HC-RD-RO Regulatory Oncology
Recruiter: Sarah Ellis
This information is for internals only. Please do not share outside of the organization.
Your Role:
As the Global Head of Medical Writing, you will shape and lead a high-performing, global function that sits at the heart of clinical development and regulatory success. In this pivotal senior leadership role, you will build, develop, and manage a team of over 100 medical writing professionals, driving the delivery of timely, high-quality clinical documentation across a complex and fast-moving global portfolio. You will set the strategic direction for medical writing standards, processes, and tools, ensuring the organization remains at the forefront of regulatory science and documentation excellence. Working in close partnership with clinical, regulatory, and vendor management stakeholders, you will translate organizational priorities into operational plans that consistently deliver results at scale. This is a rare opportunity to leave a lasting impact on how a global medical writing function operates, innovates, and elevates the quality of science that ultimately serves patients worldwide.
Location: 3x/week hybrid schedule in Billerica, MA.
Key Accountabilities:
  • Responsible for building, leading, and managing the Global Medical Writing Team (5-10 direct reports, Total staff >100)
  • Identify project staffing requirements, develop and maintain staffing plans to meet project demand
  • Ensure the delivery of timely and high-quality MW deliverables according to global project plans
  • Work closely with vendor management to ensure implementation of operating model and delivery to contracts
  • Oversee the preparation of strategies documents prepared by Medical Writing Leads, Identify gaps in skills and drive continuous improvement
  • Develop clinical documentation processes that ensure consistency and control
  • Oversee and ensure standards for clinical documents are developed, used and maintained.
  • Ensure the company follows state of the art standards / regulations / tools in medical writing activities
  • Oversee, coach and supervise vendors to ensure milestones meet timelines and deliverables are of high quality

Who You Are:
Minimum Qualifications:
  • Advanced degree in a scientific or writing discipline (Master's or PhD).
  • At least 12 years of relevant Medical Writing experience in the pharmaceutical/biotech industry.
  • A minimum of 5 years established track record managing large medical writing teams within global, matrixed organizations.
  • Ability to travel as needed.

Preferred Qualifications:
  • Demonstrated skill and engagement in state of the art medical writing tools.
  • Established track record driving the adoption of modern tools to facilitate efficient and effective medical writing.

Pay Range for this position: $234,800 - 352,200
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

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