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Clinical Writer Jobs (NOW HIRING)

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests ...

MMS

Nonclinical Writer

Raleigh, NC · On-site

Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests ...

MMS

Nonclinical Writer

Canton, MI · On-site

Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests ...

MMS

Nonclinical Writer

Boston, MA · On-site

Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests ...

Vaxcyte

Director, Clinical Medical Writing

San Carlos, CA · On-site +1

$221K - $258K/yr

Experience as lead writer for key documents included in major US and/or international regulatory ... Clear understanding of clinical development, including the phases, processes, and techniques used ...

Aequor Inc

Clinical publisher

Pittsburgh, PA · On-site

Medical Writing Clinical Publisher The primary responsibilities of the Medical Writing Clinical Publisher are to ensure the formatting quality of clinical documents including but not limited to ...

Mytonomy

Subject Matter Expert - Urology

Bethesda, MD · On-site +1

Provide clinical subject matter expertise in Urology to guide all stages of patient education content creation including: research/outlining, scripting, editing stages of video and written asset ...

Icon plc

Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

ICON

Principal Medical Writer

Blue Bell, PA · On-site +1

Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Icon plc

Principal Medical Writer

Blue Bell, PA · On-site

Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Icon plc

Principal Medical Writer

Blue Bell, PA

Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

ICON

Principal Medical Writer

Blue Bell, PA · On-site +1

Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Icon plc

Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

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Clinical Writer information

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$25

$54

$83

How much do clinical writer jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for clinical writer in the United States is $54.35, according to ZipRecruiter salary data. Most workers in this role earn between $39.90 and $64.18 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Writer, you need a solid background in life sciences or medical fields, excellent writing skills, and attention to detail, often supported by a relevant degree. Familiarity with regulatory guidelines, literature databases, and tools like EndNote, as well as certifications such as AMWA or EMWA, are highly valued. Strong communication, critical thinking, and time management help Clinical Writers convey complex information clearly and collaborate with medical professionals. These skills ensure the accuracy, clarity, and compliance of clinical documents critical for regulatory submissions and advancing medical knowledge.

What qualifications are needed to be a medical writer?

A clinical writer typically needs a strong background in life sciences, such as a degree in medicine, pharmacy, biology, or related fields. Relevant skills include excellent writing, understanding of regulatory guidelines, and familiarity with medical terminology; certifications like the Certified Medical Publication Professional (CMPP) can also enhance qualifications.

What does a clinical writer do?

A clinical writer creates scientific and regulatory documents for healthcare and pharmaceutical industries, such as clinical study reports, protocols, and regulatory submissions. They ensure accuracy, clarity, and compliance with industry standards, often working with data from clinical trials and using tools like Microsoft Word and reference management software.

How to get into medical writing with no experience?

Clinical writers often start with a background in life sciences, healthcare, or related fields, and develop skills in scientific communication, regulatory writing, and familiarity with industry guidelines. Gaining experience through online courses, certifications, or freelance projects can help build a portfolio and demonstrate competence to employers.

Is there a demand for medical writers?

There is strong demand for clinical writers, especially those with expertise in regulatory writing, medical research, and scientific communication. The healthcare and pharmaceutical industries regularly seek qualified medical writers to prepare clinical trial reports, regulatory submissions, and scientific publications, making it a growing field with diverse opportunities.

What is a Clinical Writer?

A Clinical Writer is a professional who creates, edits, and manages medical and scientific documents related to clinical research, healthcare, and pharmaceuticals. They often prepare clinical study reports, regulatory submissions, patient information leaflets, and scientific manuscripts. Clinical Writers work closely with researchers, physicians, and regulatory professionals to ensure that complex clinical information is communicated clearly, accurately, and in compliance with industry standards. Their work is essential for documenting clinical trials and supporting the approval of new drugs or therapies.

What are some common challenges clinical writers face when translating complex medical research into accessible documents?

Clinical writers often encounter the challenge of interpreting highly technical and data-rich research while ensuring accuracy and regulatory compliance. Balancing the need for scientific precision with the ability to communicate information clearly to various audiences—such as healthcare professionals, regulatory agencies, or patients—requires strong analytical and communication skills. Additionally, clinical writers must stay updated on evolving guidelines and collaborate closely with subject matter experts, which can be demanding but also enriches their expertise and professional network.
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Clinical Writer jobs near you
Infographic showing various Clinical Writer job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 5% Full Time, 92% Part Time, and 1% Temporary. Highlights an 61% Physical, 2% Hybrid, and 37% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.
Nonclinical Writer

Nonclinical Writer

MMS Holdings Inc.

Canton, MI • On-site

Full-time

Posted 2 days ago

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position.
Roles and Responsibilities:
  • Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator's Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs)
  • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical documents, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity
  • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data
  • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents
  • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports)
  • Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC
  • Demonstrated ability to lead others to complete complex projects
  • Ability to complete documents according to sponsor's format, processes, and according to regulatory guidelines
  • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment
  • Organizational expert within the nonclinical subject area
  • Excellent written/oral communication and strong time and project management skills
  • Ability to attend regular team meetings, lead client meeting and CRMs
  • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars
  • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP)
Requirements:
  • BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control
  • Knowledge of GLP, ICH guidelines, and applicable regulatory requirements
  • 2+ years of pharmaceutical regulatory nonclinical writing experience
  • Strong writing and analytical skills
  • Proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred
  • Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process

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