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Contract Medical Writing Jobs (NOW HIRING)

Global Head, Medical Writing

Billerica, MA · On-site

$234K - $352K/yr

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 ...

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 ...

Minimum of 5 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Minimum of 5 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Minimum of 5 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Minimum of 5 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Minimum of 5 years of medical writing experience in a contract research organization or pharmaceutical/biotechnology research setting. Other professional and/or educational experience may contribute ...

Minimum of 5 years of experience in writing clinical and/or regulatory documents for drugs, biologics, and/or medical devices/diagnostics for a contract research organization, pharmaceutical company ...

Support of data review and medical writing for protocols and study specific reports (regulatory ... Contract; Part time, Hourly COMMITMENTS: * Hourly as project requires * Willing to work in shifts ...

Support of data review and medical writing for protocols and study specific reports (regulatory ... Contract; Part time, Hourly COMMITMENTS: * Hourly as project requires * Willing to work in shifts ...

Support of data review and medical writing for protocols and study specific reports (regulatory ... Contract; Part time, Hourly COMMITMENTS: * Hourly as project requires * Willing to work in shifts ...

Support of data review and medical writing for protocols and study specific reports (regulatory ... Contract; Part time, Hourly COMMITMENTS: * Hourly as project requires * Willing to work in shifts ...

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Contract Medical Writing information

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$46

$78

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:
What states have the most Contract Medical Writing jobs? States with the most job openings for Contract Medical Writing jobs include:
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 Director, Medical Writing

Ideayabio

San Diego, CA

Full-time

Medical, Dental, Vision, Retirement

Posted 4 days ago


Job description

Non-Solicitation Policy and Notice to Agencies and Recruiters:

IDEAYA's Non-Solicitation Policy strictly prohibits agencies and recruiters from any contact and communication with IDEAYA employees, managers, and leaders to submit unsolicited candidate resumes and/or to solicit business partnerships. Submission of unsolicited candidate resumes by agencies or recruiters with or without a contract in place with IDEAYA Biosciences Inc. will not create any implied obligation. Failure to comply with this policy will result in disqualification from current and future business opportunities with IDEAYA Biosciences. All recruiting and talent agency decisions are strictly managed by the internal IDEAYA Human Resources function. All communication by external agencies and recruiters must be directed to humanresources@ideayabio.com. We ask that you only email your interest once.

Job Summary

About IDEAYA Biosciences:
IDEAYA is a precision medicine oncology company committed to the discovery, development, and commercialization of transformative therapies for cancer. Our approach integrates expertise in small-molecule drug discovery, structural biology and bioinformatics with robust internal capabilities in identifying and validating translational biomarkers to develop tailored, potentially first-in-class targeted therapies aligned to the genetic drivers of disease. We have built a deep pipeline of product candidates focused on synthetic lethality and antibody-drug conjugates, or ADCs, for molecularly defined solid tumor indications. Our mission is to bring forth the next wave of precision oncology therapies that are more selective, more effective, and deeply personalized with the goal of altering the course of disease and improving clinical outcomes for patients with cancer.
When you're at IDEAYA, you will be in the midst of brilliant minds working on precision medicine therapies to help cancer patients. We are passionate and committed about being on the forefront of oncology medicine, which means we all have a high internal drive that is at the very core of every person at IDEAYA. We are inquisitive, ask deep questions, and are data-driven innovators who like to collaborate and use team work to move science forward. For more information, please see www.ideayabio.com.
Location: South San Francisco
Position Summary:
IDEAYA is seeking a highly motivated, well-organized, and skilled Senior Director, Medical Writing to provide strategic and operational leadership across oncology programs spanning early- and late-stage development. This role is responsible for delivering high-quality regulatory and clinical documents that support global development and registration strategies.
You will partner closely with Clinical Development, Regulatory Affairs, Biometrics, and Clinical Operations to ensure scientifically rigorous, compliant, and timely documentation. The ideal candidate brings deep oncology expertise, including familiarity with complex trial designs, endpoints (e.g., ORR, PFS, OS), and evolving regulatory expectations.
Level will be commensurate with experience.
This position is based in our South San Francisco headquarter or San Diego office and required to be onsite four days per week per our company policy.
Reporting to: Senior Vice President, Medical Writing and Project Management

Job Description

What you'll do:

  • Lead authoring strategy and oversee the successful development ofclinical and regulatory documents (e.g., INDs, NDAs, BLAs, MAAs, Protocols, IBs/DSURs, CSRs, Briefing Documents) in accordance with applicable global regulatory requirements
  • Translate complex oncology and biomarker-driven data into clear, scientifically accurate, compliant, submission-ready documentation
  • Plan and manage medical writing activities, timelines, and resources across multiple programs
  • Lead cross-functional document reviews, resolve feedback, and drive documents to approval
  • Work effectively with cross-functional teams by creating an atmosphere of openness and trust
  • Oversee vendors, budgets and resources for medical writing
  • Lead a medical writing team to successfully meet the portfolio needs

Requirements:

  • Advanced degree (PhD, PharmD, MD, or MS) in life sciences
  • 10-12 years of medical writing experience, in biotech/pharmaceutical industry, including 5+ years in a leadership role supervising a medical writing team
  • Proven leadership experience supporting INDs and at least one major regulatory submission in oncology
  • Demonstrated expertise in authoring and overseeing a broad range of clinical and regulatory documents
  • Strong knowledge of global regulatory requirements (ICH, GCP, CTD/eCTD)
  • Proven ability to manage complex projects and influence cross-functional teams
  • Experience managing direct reports, contractors, and/or vendors
  • Excellent written and verbal communication skills
  • Experience with innovative technologies to expedite document preparation (e.g., artificial intelligence tools)
  • Experience working in small to mid-sized biotech or fast-growth environments with novel oncology modalities
  • Advanced knowledge of scientific medical writing principles, tools and practices in oncology.
  • Strategic thinking, scientific rigor, strong leadership and team development with high attention to detail and quality focus.
  • Strong interpersonal skills, including excellent written and effective communication skills with senior stakeholders which are essential in this collaborative work environment.
  • Self-motivated, with initiative and the ability to take ownership of, and follow through on specific tasks, initiatives or programs.
  • Ability to manage multiple priorities in a fast-paced environment
  • Staff development experience a plus.

All employees are expected to act with integrity and in full compliance with applicable laws, regulations, and IDEAYA policies, including IDEAYA's Code of Conduct.

Employees must demonstrate good judgement and ethical behavior in all business activities, maintain patient and product safety as a top priority, and report any suspected violations of law or Company policy through appropriate channels

Total Rewards

Along with our inspiring mission, and highly collaborative and inclusive environment, IDEAYA offers a competitive total rewards package that reflects our pay-for-performance philosophy where employees are eligible to be considered for merit-based salary increases, company discretionary short-term incentive plan participation, and company discretionary stock option awards (based on board approval). Our comprehensive benefits package includes, but is not limited to, medical/dental/vision coverage (100% company paid for employees and 90% company paid for dependents), 401k, ESPP, and wellness programs.

The expected salary range for the roleof Senior Director, Medical Writing is $ $245,000 - $302,000. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the office location where this open position is located, the final candidates' experience within their profession, experience in the disease areas we are striving to make an impact in as a company, length of time within the industry, educational background, and performance during the interview process.

The Company complies with all laws respecting equal employment opportunities and does not discriminate against applicants with regard to any protected characteristic as defined by federal, state, and local law. This position requires you to work onsite in the office at the Company's facilities for training & meetings, with work-from-home flexibility, and the Company requires that all employees working in its facilities be fully vaccinated (except as required by applicable law). Therefore, this position requires you to be fully vaccinated from COVID-19, subject to reasonable accommodations for medical or religious reasons, and/or as otherwise required by applicable law. The Company considers you fully vaccinated once 14 days have passed since you received either the second dose in a two-dose COVID-19 vaccine series or a single-dose COVID-19 vaccine. The vaccine must have been FDA approved, have emergency use authorization from the FDA, or, for persons fully vaccinated outside of the U.S., be listed for emergency use by the World Health Organization.

IDEAYA is an equal opportunity employer. In accordance with applicable law, IDEAYA does not discriminate in hiring or otherwise in employment based on race, color, religion, sex, national origin, age, marital or veteran status, disability, sexual orientation, or any other legally protected status. EOE/AA/Vets.

We are committed to providing reasonable accommodations to qualified individuals with disabilities. If you need assistance or an accommodation due to a disability, please get in touch with us at hr@ideayabio.com.