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Remote Clinical Evaluation Report Writer Jobs (NOW HIRING)

Miller Cooper

Super Set Report Writer

Winter Park, FL · Remote

This is a remote position. About National Quality Systems National Quality Systems (NQS) is a ... NQS builds and supports clinical registry platforms serving trauma, burn, and emergency general ...

Lynn University

Workday Report Writer

The fully remote Research Analyst position reports to the Director of Institutional Research ... Responsibilities include querying internal databases; manipulating and evaluating data; filling ad ...

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

... generation of Clinical Evaluation Reports (CER) and associated documentation. Specifically ... Writes and or edits clinical study documentation, including clinical investigational plans ...

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

... generation of Clinical Evaluation Reports (CER) and associated documentation. Specifically ... Writes and or edits clinical study documentation, including clinical investigational plans ...

Prosper Health

Remote Clinical Psychologist

Weston, FL · On-site +1

$100K - $120K/yr

... evaluations and develop personalized post-assessment plans * Write clear, thorough clinical reports ... Proficient remote communication abilities * Tech competence and self-direction * Desire to support ...

Rockstar

Remote Clinical Psychologist

$90K - $124K/yr

... evaluations and develop personalized post-assessment plans * Write clear, thorough clinical reports ... Proficient remote communication abilities * Tech competence and self-direction * Desire to support ...

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Remote Clinical Evaluation Report Writer information

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How much do remote clinical evaluation report writer jobs pay per year?

As of Jul 18, 2026, the average yearly pay for remote clinical evaluation report writer in the United States is $78,865.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $102,000.00 per year, depending on experience, location, and employer.

What is a Remote Clinical Evaluation Report Writer?

A Remote Clinical Evaluation Report Writer is a professional who prepares detailed reports evaluating the clinical data and safety of medical devices, typically working from a remote location. Their main responsibility is to assess and summarize clinical evidence to support regulatory submissions and ensure medical devices comply with relevant standards and regulations. They collaborate with clinical experts, regulatory teams, and manufacturers to gather and analyze data, and then draft comprehensive Clinical Evaluation Reports (CERs) as required by authorities like the EU MDR. Strong writing, analytical skills, and knowledge of medical device regulations are essential for this role.

What is the difference between Remote Clinical Evaluation Report Writer vs Remote Medical Writer?

AspectRemote Clinical Evaluation Report WriterRemote Medical Writer
CredentialsTypically requires clinical or healthcare-related certifications, such as RN, MD, or clinical research certificationsUsually requires medical, scientific, or regulatory writing certifications or degrees
Work EnvironmentPrimarily focused on evaluating clinical data and writing reports for regulatory submissionsCreates a variety of medical documents, including manuscripts, regulatory documents, and marketing materials
Industry UsageCommonly employed in regulatory affairs, clinical research organizations, and pharmaceutical companiesUsed across pharmaceutical, biotech, and medical device industries for scientific communication

The main difference is that Remote Clinical Evaluation Report Writers focus on analyzing clinical data and preparing evaluation reports for regulatory purposes, while Remote Medical Writers produce a broader range of medical documents for scientific and marketing communication. Both roles require strong medical knowledge and writing skills but serve different functions within the healthcare industry.

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

To thrive as a Remote Clinical Evaluation Report Writer, you need a background in life sciences, strong analytical skills, and experience in regulatory writing, often supported by a relevant degree. Familiarity with medical device regulations (such as MDR), literature review databases, and proficiency in document management systems are typically required. Exceptional attention to detail, time management, and clear written communication distinguish outstanding professionals in this role. These skills ensure the production of accurate, compliant, and persuasive clinical evaluation reports crucial for medical device approval and market access.

How does a Remote Clinical Evaluation Report Writer typically collaborate with medical and regulatory teams during the report-writing process?

As a Remote Clinical Evaluation Report (CER) Writer, you frequently interact with clinical experts, regulatory affairs professionals, and sometimes product development teams to gather and clarify essential data for your reports. Collaboration is often conducted via virtual meetings, emails, and shared document platforms to ensure alignment on regulatory requirements and clinical evidence. You may also participate in cross-functional review sessions to address feedback and make revisions. This collaborative approach is crucial to ensure that the final CER meets both internal quality standards and external regulatory expectations.
More about Remote Clinical Evaluation Report Writer jobs
What cities are hiring for Remote Clinical Evaluation Report Writer jobs? Cities with the most Remote Clinical Evaluation Report Writer job openings:
What are the most commonly searched types of Clinical Evaluation Report Writer jobs? The most popular types of Clinical Evaluation Report Writer jobs are:
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Remote Clinical Evaluation Report Writer jobs near you
Infographic showing various Remote Clinical Evaluation Report Writer job openings in the United States as of July 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 100% Remote job distribution, with an average salary of $78,865 per year, or $37.9 per hour.

Clinical Evaluation Report Medical Writer (1099 Contractor)

Criterion Edge Professional Services Inc.

Los Angeles, CA • Remote

Contractor

Re-posted 20 days ago

Job description

Medical Writer 

Criterion Edge is seeking a remote candidate for the role of Medical Writer to join our best-in-class writing team and help take our customer focused writing services to new heights.  

Employment Type and Location:  Remote 1099 Contractor (Part Time/Full Time) 

Job Overview  

In the role of Medical Writer, you will have the opportunity to work closely with other writers, project managers and support specialists to produce a wide variety of regulatory and scientific reports, plans, and other written deliverables for medical device, pharma/biotech, and in vitro device clients. 

The ideal candidate is a writing professional looking to build on their relevant medical writing experience, scientific knowledge, and well-developed written and oral communication skills. We value proactive thinkers with the ability and desire to work in a multifunctional team setting, producing documents and reports that align with the highest regulatory, scientific, and professional standards. 

Roles and Responsibilities  

As a member of our project writing team, you will be responsible for producing assigned written documents and reports to a high standard.  Your specific responsibilities include: 

  • Direct responsibility for writing documents or document sections on assigned projects. 

  • Able to organize own project workload and tasks, identify project needs and adhere to project timelines.  

  • Understand client expectations and work to meet those expectations through teamwork, adherence to deadlines, problem-solving and scientific knowledge.  

  • Effectively collaborate with other members of the project writing team.  

  • Working with a Criterion Edge Project Manager, document your assigned tasks, time estimates and due dates into the Asana project plan. Provide weekly progress updates. 

  • Ensure all data presented in the document are clear, complete, accurate, and concise. Ensure all statements and conclusions are integrated, balanced, supported by appropriate data, and consistent across all related documents. 

  • Receive expert/scientific review comments and adjust the document content as required based on internal and external feedback. 

  • Stay abreast of current medical writing best practices and relevant regulatory knowledge.   

  • Proactively identify potential project risks and bring those forward to the overall project team to discuss and identify solutions.    

  • Participate in quality control (QC) checks for accuracy following established internal QC processes. 

  • Provide written and verbal feedback to junior staff and managers when appropriate. 

  • When requested, serve as a project mentor to assist in the training and development of junior staff on your project team(s). 

  • Establish and maintain effective, professional working relationships with co-workers, managers, and clients. 

  • Demonstrate initiative and sound judgement when faced with less familiar project requirements and/or document situations or challenges.  Seeks understanding and additional clarity from Project Lead and/or Project Management before proceeding.  

Qualifications and Skills 

  • 2+ years of direct writing experience in pharmaceutical, medical device, in vitro device or related academic fields. 

  • Minimum of a BSc in a life sciences or related discipline / related field. 

  • Advanced word processing skills, including Microsoft Office (including Word), Adobe Acrobat, Excel and collaborative document sharing platforms such as SharePoint; ability to learn and adapt to various IT systems. 

  • Familiar with all current and applicable guidelines and regulations governing the assigned project. 

  • Knowledge of and experience with systematic literature review (SLR) methodology and best practices, including Level 1 and Level 2 literature screening, data extraction and weighting and appraisal of data sets. 

  • High level of English fluency or native English speaker, with excellent oral (including presentation) and written communication, including grammatical/technical writing skills.  

  • Able to interact confidently with external stakeholders and communicate with others effectively and clearly.  

  • Capable of working independently to achieve assigned project goals with minimal supervision. 

  • Reliably produces high-quality written deliverables in accordance with customer and project requirements and agreed timelines. 

  • Excellent attention to detail and accuracy. 

  • Contributes, collaborates, shares responsibilities, and supports other team members to ensure success with tasks/projects. 

  • Demonstrates scientific rigor and understanding of the scientific process in written documents. 

About Criterion Edge:  

At Criterion Edge, we’re committed to empowering companies to deliver better healthcare solutions. By leveraging best-in-class writing processes, technology, and experience, our expert team of writers and project managers support healthcare companies to achieve their global regulatory goals with superior quality, speed, and budget control.  

Be on the leading edge by applying your regulatory and/or scientific writing expertise and leadership skills to the development, management and writing of regulatory-compliant projects with top industry clients. 

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