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Remote Cer Writer Jobs (NOW HIRING)

LivaNova

Regulatory & Clinical Specialist

Denver, CO · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Dallas, TX · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Phoenix, AZ · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Boston, MA · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Houston, TX · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Austin, TX · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Charlotte, NC · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Chicago, IL · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

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How much do remote cer writer jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for remote cer writer in the United States is $35.11, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $50.96 per hour, depending on experience, location, and employer.

What is a Remote CER Writer?

A Remote CER Writer is a professional who specializes in creating Clinical Evaluation Reports (CERs) for medical devices, working from a remote location. CER Writers gather, analyze, and synthesize clinical data to demonstrate the safety and performance of medical devices as required by regulatory authorities like the European Medicines Agency (EMA) or FDA. They collaborate with regulatory teams, subject matter experts, and sometimes clinical researchers to ensure all documentation meets strict compliance and quality standards. Working remotely allows these professionals to perform their tasks from anywhere, using digital tools to communicate and manage documentation.

What is the difference between Remote Cer Writer vs Remote Medical Writer?

AspectRemote Cer WriterRemote Medical Writer
Required CredentialsCertification in medical writing or related fields, sometimes specific to certification bodiesMedical or life sciences degree, often with certification in medical writing
Work EnvironmentHome-based, flexible schedules, often project-basedHome-based, with collaboration in teams, deadlines for regulatory documents
Industry UsagePharmaceutical, healthcare, regulatory agenciesPharmaceutical, biotech, medical communications
Common Search/ComparisonRemote Cer Writer vs Remote Medical Writer

Remote Cer Writers focus on creating clinical and regulatory documentation for healthcare and pharmaceutical companies, often requiring certification in medical writing. Remote Medical Writers also produce scientific content but may work on a broader range of medical communications, including marketing and educational materials. Both roles are home-based, require relevant credentials, and serve the healthcare industry, but their specific focus and types of documents differ.

What are some common challenges faced by Remote CER Writers, and how can they be effectively managed?

Remote CER Writers often encounter challenges such as coordinating with global teams across different time zones, managing large volumes of scientific literature, and ensuring timely access to subject matter experts for clinical evaluation report inputs. Effective communication tools, well-organized project management systems, and proactive scheduling of virtual meetings can help mitigate these challenges. Building strong relationships with regulatory, clinical, and quality teams also facilitates smoother collaboration and ensures the CER meets stringent regulatory requirements.

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

To thrive as a Remote CER Writer, you need a strong background in scientific writing, clinical research, and regulatory knowledge, often supported by a degree in life sciences or related fields. Familiarity with regulatory guidelines (such as MDR, MEDDEV 2.7/1), literature review databases, and document management systems is essential. Attention to detail, strong organizational skills, and clear communication are vital soft skills for producing high-quality Clinical Evaluation Reports (CERs) remotely. These skills ensure regulatory compliance, clarity, and accuracy in documentation, which are critical for successful medical device approvals.
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Remote Cer Writer jobs near you

Associate Medical Writer, In Vitro Diagnostic Regulation (IVDR) Writing Services

Criterion Edge Professional Services Inc.

Los Angeles, CA • Remote

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Associate Medical Writer, In Vitro Diagnostic Regulation (IVDR) Writing Services 

Job Type: Full-Time, Remote 

Experience Level: Experienced 

At Criterion Edge, we’re committed to empowering companies to deliver better healthcare solutions. By leveraging best-in-class writing processes, technology, and expertise, we empower healthcare companies to achieve their global regulatory goals with superior quality, speed, and budget control. Be on the leading edge by applying your regulatory writing expertise and leadership skills to the development, management and writing of regulatory-compliant performance evaluation reports (PER) projects with top industry clients. 

In the role of Associate Medical Writer, you will have the opportunity to work closely with other writers, project managers and project support specialists to support and lead multiple PER writing projects that support EU IVDR submission requirements for the client’s portfolio of IVD products. Please note that previous PER or CER writing experience and management of medical regulatory writers is required for this role. 

The ideal candidate is looking to build their medical writing career and should possess basic 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 professional standards. 

Specific responsibilities include: 

As a support member on our project writing team, you will actively collaborate and work together with other members of the project writing team to produce assigned written documents and reports to a high standard.  Your specific responsibilities include: 

  • Take direction from other members of the project writing team on assigned writing tasks.  

  • Plan and organize your workload on assigned projects and tasks and adhere to established project timelines and workload estimates.  

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

  • Consistently monitor your work for accuracy and quality by following established internal QC processes. 

  • Work with Criterion Edge Project Manager to accurately document your assigned project tasks, task timeline estimates and assignments into the project plan. Provide weekly progress updates. 

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

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

  • Attend internal meetings as needed.   

  • Required Experience: 

  • Previous experience writing CERs and/or PERs and related documents in accordance with MEDDEV 2.7/1 rev 4 and/or EU MDR and/or EU IVDR 

  • Effective written, verbal and presentation skills in technical/laboratory diagnostics 

  • Strong command of medical and laboratory terminology 

  • Demonstrated ability to identify and adapt to shifting priorities and competing demands 

  • Skilled in document development and management using Word, Excel, PowerPoint and EndNote 

  • Training and degree in science, engineering, or medical field(s). Scientific/research background required, with a deep understanding of research design, methodology, and statistics 

If interested, please submit a resume/CV and a cover letter to careers@criterionedge.com. For more job openings, check out our careers page.  

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