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Medical Writing Jobs (NOW HIRING)

Alkermes

Associate Director, Medical Writing

Waltham, MA · Hybrid

$175K - $190K/yr

The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities across one or more clinical development programs. This role combines hands-on ...

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You will oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations. Key responsibilities include: * Leading the preparation and review of clinical study ...

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Principal Medical Writer

Blue Bell, PA

You will oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations. Key responsibilities include: * Leading the preparation and review of clinical study ...

Icon plc

Principal Medical Writer

Blue Bell, PA

You will oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations. Key responsibilities include: * Leading the preparation and review of clinical study ...

ICON

Principal Medical Writer

Blue Bell, PA · On-site +1

You will oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations. Key responsibilities include: * Leading the preparation and review of clinical study ...

Prometrika LLC

Senior Medical Writer

Cambridge, MA · On-site

$134K - $162K/yr

PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. We're ...

IQVIA

Senior Medical Writer

Durham, NC

Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments. Provides written and verbal feedback to junior staff, and to ...

Medasource

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

This role requires advanced medical writing skills, deep knowledge of regulatory requirements, the ability to mentor junior writers, and strong interpersonal and presentation abilities. Candidates ...

Syneoshealth

Medical Writer II - Publications

OR · Remote

Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments ...

ProPharma Group

Senior Medical Writer

Charleston, WV

Strives to complete medical writing deliverables on time and within budget. * With minimal supervision, manages client expectations and interacts and communicates directly with clients, leads team ...

BioMarin Pharmaceutical Inc.

Senior Medical Writer

Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams). * Builds effective partnerships with cross-functional groups to ensure customer ...

BioMarin Pharmaceutical Inc.

Senior Medical Writer

Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams). * Builds effective partnerships with cross-functional groups to ensure customer ...

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Medical Writing information

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$46

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How much do medical writing jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for 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.

Will medical writing jobs be replaced by AI?

Medical writing jobs involve creating complex, accurate, and compliant scientific content, which currently requires human expertise in understanding medical data, regulations, and audience needs. While AI tools can assist with drafting and editing, they are unlikely to fully replace medical writers due to the need for critical thinking, ethical judgment, and nuanced communication. Professionals in this field will benefit from integrating AI as a supportive tool rather than a replacement.

What is medical writing?

Medical writing is the process of creating scientific documents by specialized writers in the healthcare, pharmaceutical, or biotechnology industries. These documents can include clinical trial reports, regulatory submissions, research manuscripts, patient education materials, and more. Medical writers must accurately present complex medical information in a clear, concise, and compliant manner, often working closely with researchers, doctors, and regulatory professionals. The role requires a strong understanding of medical terminology, scientific research, and regulatory guidelines.

How do I become a medical writer?

To become a medical writer, typically a bachelor's degree in life sciences, healthcare, or a related field is required, often supplemented by advanced degrees or certifications in medical writing or regulatory writing. Gaining experience through internships, developing strong writing skills, and becoming familiar with medical terminology, clinical trial processes, and regulatory guidelines such as ICH or FDA standards are important steps. Proficiency with tools like Microsoft Word and reference management software also supports success in this field.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals or those with specialized skills can earn over $100,000 per year. The role often requires strong writing skills, knowledge of medical terminology, and familiarity with regulatory guidelines.

What is the difference between Medical Writing vs Medical Editing?

AspectMedical WritingMedical Editing
Required CredentialsTypically requires a background in life sciences, healthcare, or related fields; often a degree or certification in medical writingRequires strong knowledge of medical terminology and writing; often a background in healthcare, editing, or related fields
Work EnvironmentOften works independently or in teams, creating clinical documents, regulatory submissions, and educational materialsUsually works alongside writers, reviewing and refining medical documents for clarity, accuracy, and consistency
Employer & Industry UsageUsed in pharmaceutical, biotech, healthcare, and medical device industriesCommon in publishing, healthcare communications, and regulatory agencies

Medical Writing involves creating original medical content such as clinical study reports, regulatory documents, and educational materials. Medical Editing focuses on reviewing and refining these documents to ensure clarity, accuracy, and compliance. Both roles require strong medical knowledge, but Medical Writers produce content, while Medical Editors improve existing content.

What is a medical writer?

A medical writer is a professional who creates scientific documents such as research articles, regulatory submissions, and clinical trial reports. They combine expertise in medicine and writing skills to communicate complex medical information clearly and accurately, often working with healthcare professionals and using tools like reference management software.

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

To thrive as a Medical Writer, you need strong scientific knowledge, excellent written communication skills, and typically a background in life sciences or healthcare. Familiarity with referencing software, regulatory guidelines, and document management systems is often required. Attention to detail, adaptability, and the ability to explain complex concepts clearly are valuable soft skills in this role. These abilities ensure the accurate and effective communication of medical information for regulatory, clinical, or educational purposes.

How does a medical writer typically collaborate with subject matter experts and regulatory teams during a project?

Medical writers regularly interact with subject matter experts (such as clinicians and researchers) to ensure scientific accuracy and clarity in documents like clinical study reports, publications, or regulatory submissions. They also work closely with regulatory teams to align content with current guidelines and submission requirements. This collaboration often involves attending meetings, managing document reviews, and incorporating diverse feedback to produce high-quality, compliant deliverables. Effective communication and project management skills are essential to coordinate these multi-disciplinary efforts and meet strict deadlines.

What Are Medical Writing Jobs?

Medical writing jobs work in health care and science communities to compose documents and articles. Those who have medical writing jobs may draft many different kinds of papers, such as educational or promotional literature, medical abstracts for textbooks, or research documents. Other medical writing jobs include ghost-writing for prominent scientists or physicians, journalistic writing for scientific magazines, or creating content for marketing materials. Regardless of what field you are in, to obtain medical writing jobs, you must be able to decipher and interpret complicated information and write in a manner that your audience understands. For example, you may use medical jargon in scientific journals, but medical writers typically use simpler language when writing for the general public.

More about Medical Writing jobs
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Medical Writing jobs near you
Associate Director, Medical Writing

Associate Director, Medical Writing

Alkermes

Waltham, MA • Hybrid

$175K - $190K/yr

Full-time

Posted 15 days ago

Key responsibilities

  • Provide strategic and operational leadership for medical writing activities across clinical development programs.

  • Independently author and lead the planning, review, comment resolution, and delivery of clinical and regulatory documents.

  • Lead or coordinate clinical content development for complex regulatory submissions, ensuring alignment with regulatory strategy and development objectives.

Job description

The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities across one or more clinical development programs. This role combines hands-on writing expertise with responsibilities for resource planning and matrix leadership to deliver high-quality, fit-for-purpose clinical and regulatory documents aligned with program and regulatory objectives. The Associate Director is accountable for document development strategy, planning, and execution; leads clinical content development for complex submissions (including content strategy, organization, and resourcing); and partners with Clinical Development, Regulatory Affairs, Biostatistics, and other key functions to ensure cohesive messaging, mitigate risk, and support successful regulatory interactions and filings. The Associate Director applies advanced technical judgment to solve complex problems and ensures Medical Writing activities are integrated with broader development and regulatory objectives.

Why join Team Alkermes?

Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.

We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. 

Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law.  Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Alkermes is an E-Verify employer.

  • Advanced degree (PhD, PharmD, or equivalent) in a relevant discipline.

  • 8+ years of relevant experience in medical writing, clinical research, or a related function.

  • Experience supporting marketing authorization applications (NDA/BLA/MAA), IND submissions, and other major regulatory filings.
  • Demonstrated ability to lead complex projects, plan and optimize resources (internal staff, vendors, and tools), and manage competing priorities.

  • Strong ability to work independently, navigate ambiguity, and resolve complex, non-routine problems through pragmatic risk mitigation.

  • Broad scientific understanding across multiple therapeutic areas; neuroscience experience preferred but not required.

  • Excellent written and verbal communication skills, with proven ability to influence and collaborate across diverse teams.

Alkermes has recently adopted a hybrid working environment to support and meet the needs of employees and this role will operate in a flexible environment with 60% of time in the office and 40% from home. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote work. 

The annual base salary for this position ranges from $175,000 - $190,000. In addition, this position is eligible for an annual performance pay bonus.  Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package.  Additional details can be found on our careers website: www.alkermes.com/careers#working-here  

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  • Accountable for medical writing deliverables across one or more clinical programs, contributing to program-level plans and ensuring aligned timelines, quality, and resourcing.

  • Independently author and lead the planning, review, comment resolution, and delivery of routine and complex clinical and regulatory documents.

  • Lead or coordinate clinical content development for complex regulatory submissions, ensuring messaging alignment with regulatory strategy and development objectives.

  • Serve as the primary medical writing lead on program teams, proactively identifying risks, anticipating cross-functional challenges, and driving issue resolution.

  • Oversee outsourced writing support, setting expectations, managing review cycles, and ensuring inspection-ready quality.

  • Contribute to the development and execution of Medical Writing departmental goals, including process improvements, inspection readiness initiatives, and adoption of new tools and technologies.

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