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Remote Clinical Evaluation Report Writer Jobs (NOW HIRING)

Horizontal Talent

Sr. Medical Writer

Libertyville, IL · On-site +1

$36 - $70/hr

This role is ideal for a detail-oriented medical writer who enjoys turning complex clinical ... Prior experience creating Clinical Evaluation Reports and related regulatory documents.

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF ...

Murj

Remote Clinical Specialist

Remote Clinical Specialists are essential to Murj's Remote Clinical Services model and directly ... reporting, and No action required * Exercise independent clinical judgment when evaluating ...

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF ...

Stryker

Senior Staff Medical Writer (Remote)

Phoenix, AZ · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF ...

Stryker

Senior Staff Medical Writer (Remote)

Seattle, WA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF ...

Stryker

Senior Staff Medical Writer (Remote)

San Diego, CA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF ...

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF ...

Solventum

Medical Writer - Clinical Compliance

$124K - $170K/yr

Authoring and coordinating Clinical Evaluation Plans and Clinical Evaluation Reports (CEPs/CERs ... Remote - United States Travel: May include up to 10% domestic Relocation Assistance: Not authorized ...

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 ...

Zeiders Enterprises

Remote Clinical Counselor

$60K - $80K/yr

Report suspected child abuse and domestic abuse/violence to the local civilian authorities and the ... Proficiency in oral and written communication skills * Knowledge of Microsoft Office Suite software ...

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 ...

Pharmacy Careers

Remote Clinical Review Pharmacist

$121K - $144K/yr

Excellent clinical writing, critical thinking, and communication. Why This Role? * 100% remote with flexible scheduling. * Help patients access safe, effective, and affordable medications. * Develop ...

Pharmacy Careers

Remote Clinical Review Pharmacist

$121K - $144K/yr

Excellent clinical writing, critical thinking, and communication. Why This Role? * 100% remote with flexible scheduling. * Help patients access safe, effective, and affordable medications. * Develop ...

Pharmacy Careers

Remote Clinical Review Pharmacist

$121K - $144K/yr

Excellent clinical writing, critical thinking, and communication. Why This Role? * 100% remote with flexible scheduling. * Help patients access safe, effective, and affordable medications. * Develop ...

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Remote Clinical Evaluation Report Writer information

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$42K

$78.9K

$136K

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

As of Sep 2, 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.

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.

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.

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.

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:

What states have the most Remote Clinical Evaluation Report Writer jobs?

States with the most job openings for Remote Clinical Evaluation Report Writer jobs include:

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The top searched job categories for Remote Clinical Evaluation Report Writer jobs are:

Remote Clinical Evaluation Report Writer jobs near you
Infographic showing various Remote Clinical Evaluation Report Writer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,865 per year, or $37.9 per hour.

Sr. Medical Writer

Horizontal Talent

Libertyville, IL • On-site, Remote

$36 - $70/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 6 days ago

Job description

Join a dynamic regulatory clinical evaluation team supporting the development and life cycle of vascular medical devices. This role is ideal for a detail-oriented medical writer who enjoys turning complex clinical, scientific, and regulatory information into high-quality documentation that supports product submissions and compliance.

Responsibilities
  • Develop and refine clinical evaluation deliverables, including Clinical Evaluation Plans, Clinical Evaluation Reports, SSCPs, regulatory responses, and related documentation.
  • Review and synthesize evidence from clinical studies, published literature, post-market surveillance, risk documentation, and post-market clinical evaluations.
  • Support product applications and submissions by analyzing clinical data and preparing clear, accurate written materials.
  • Collaborate with cross-functional partners across regulatory affairs, quality, clinical affairs, engineering, risk management, medical affairs, sales, marketing, and other stakeholder groups.
  • Maintain familiarity with assigned products and incorporate relevant information from a wide range of technical and clinical sources.
  • Review IFUs, patient materials, training content, risk files, protocols, plans, and reports to help ensure consistency and alignment.
  • Contribute to responses to complex questions from external stakeholders and regulatory bodies.
  • Ensure documentation quality, accuracy, consistency, and compliance with applicable policies, procedures, regulations, and guidance.
Skills
  • Bachelor’s degree or an equivalent combination of education and work experience.
  • 6–8 years of medical writing experience in the medical or pharmaceutical industry, or 8+ years of general technical writing experience.
  • Experience writing in a medical, pharmaceutical, medical device, clinical research, or related environment.
  • Strong written and verbal communication skills with the ability to explain complex information clearly.
  • Excellent analytical skills and the ability to manage multiple priorities and deadlines effectively.
  • Comfort working in collaborative, cross-functional team settings.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
  • Ability to produce accurate work with strong attention to detail and consistency.
Preferred Skills
  • Background in biomedical science, medicine, or another health-related discipline.
  • Prior experience creating Clinical Evaluation Reports and related regulatory documents.
  • Familiarity with clinical study design, clinical study management, quality engineering, or risk management.
  • Experience working with medical device regulatory requirements and guidance, including ISO 13485, ISO 14155, ISO 14791, MEDDEV 2.7.1, MDR, and FDA/EU guidance.
  • Ability to support responses to regulatory inquiries and external questions with sound judgment and professionalism.

Horizontal is committed to fostering an inclusive workplace where diversity, equity, and belonging are valued. We welcome candidates with a wide range of backgrounds, experiences, and perspectives, and we encourage everyone to apply if they meet the core requirements of the role.

By applying for this position, you acknowledge and agree that Horizontal Talent may contact you regarding your application using automated technology, including phone calls, SMS/text messages, or email, which may be delivered by our virtual AI recruiter, Alex.


Please apply through this online posting or by visiting our Job Board at www.horizontaltalent.com/job-board. Applications will be accepted for 4 weeks. For those that join the team, we offer competitive compensation and benefits including medical, dental, vision, and retirement. Check out all we have to offer and how you can become part of the Horizontal Talent Team. The pay range for this role is $36 - $70 per hour based on qualifications and experience.

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