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Clinical Writer Jobs (NOW HIRING)

Laborie

Medical Writer II

Plymouth, MN · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Laborie

Medical Writer II

Salt Lake City, UT · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Laborie

Medical Writer II

Mechanicsburg, PA · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Sobi

Principal Medical Writer

San Diego, CA · Hybrid

... Writer, you will provide communication expertise and lead a strategy-driven approach to authoring ... Assume primary responsibility for preparation of key clinical and regulatory documents and ...

Sobi

Principal Medical Writer

San Diego, CA · On-site

... Writer, you will provide communication expertise and lead a strategy-driven approach to authoring ... Assume primary responsibility for preparation of key clinical and regulatory documents and ...

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Clinical Writer information

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$25

$54

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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.
Medical Writer II

Medical Writer II

Laborie Medical Technologies Corp

Plymouth, MN • Hybrid

$115K - $125K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 28 days ago

Job description

We believe that great healthcare is an essential safeguard of human dignity.
At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.
 
We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.
 
Who We’re Looking For:
The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and scientific conferences and meetings. This involves collaboration with internal and external partners to support technical, medical, and clinical writing functions for Clinical and Regulatory business needs in accordance with the relevant standards as well as LABORIE standard operating procedures. This person will write a variety of documents for distinct audiences including Post-Market Surveillance plans and reports, clinical evaluation plans and reports, reports and study protocols, and may assist with the development of instructions for use and other product labeling that requires the presentation of medical information. 
 
About the Role:
  • Performs online literature searches, manage the literature database, and prepare literature reviews to support LABORIE's products.
  • Critically appraise, analyze, and summarize data from experiments, clinical trials, and publications in the support of appropriate device claims, indications, publications, and clinical evaluation reports (CERs) and Clinical Study Reports (CSRs). 
  • Search out, review, write and maintain records of post market surveillance (PMS) data pertaining to the safety and effectiveness of LABORIE devices. 
  • Research, create, and edit scientific documents and presentations to and from the internal team, KOLs, investigators, and physicians.
  • Assist in ensuring all clinical requirements are met for device registrations and maintenance while working with other LABORIE team members.
  • Undertake various projects and tasks as assigned.
Minimum Qualifications:
  • Bachelor's degree in a scientific field or in writing/composition discipline and 5+ years' experience in medical or technical writing.
  • Experience in Clinical Evaluation Reports and similar technical documentation in accordance with MEDDEV 2.7/1 Rev 4 and MDR Submissions.
  • Working knowledge of medical device clinical regulations, standards and guidelines (ISO, MEDDEV, MDR, IVDR, FDA CFR) and experience conducting focused literature searches on PubMed, Embase, Google Scholar, or other similar medical literature databases. 
  • Demonstrated ability to manage project timelines, including ability to adapt to shifting priorities and competing demands while maintaining strong attention to detail. 
  • Strong computer skills, proficiency in MS Office and ability to work both independently and collaboratively in a team setting. 
  • Excellent English verbal and written presentation skills, with great attention to detail. 
  • Experience working in the medical device industry preferred. 
  • Project Management experience preferred. 
Why Laborie:
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
  • Paid time off and paid volunteer time
  • Medical, Dental, Vision and Flexible Spending Account
  • Health Savings Account with Company Funded Contributions
  • 401k Retirement Plan with Company Match
  • Parental Leave and Adoption Services
  • Health and Wellness Programs and Events
  • Awarded 2025 Cigna Healthy Workforce Designation Gold Level
Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.
 
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