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Commission Clinical Evaluation Report Writer Jobs

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 ...

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$42K

$78.9K

$136K

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

As of Sep 8, 2026, the average yearly pay for commission 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 commission clinical evaluation report writer?

A Commission Clinical Evaluation Report Writer is a professional who prepares clinical evaluation reports (CERs) required for medical device regulatory submissions, particularly under the European Union Medical Device Regulation (EU MDR). Their main responsibility is to analyze and present clinical data, scientific literature, and risk-benefit information to demonstrate the safety and performance of medical devices. They work closely with regulatory, clinical, and engineering teams to ensure that CERs meet all compliance requirements. Their work is essential for getting medical devices approved for market entry. Strong writing, research, and regulatory knowledge are crucial skills for this role.

What are the key skills and qualifications needed to thrive as a commission clinical evaluation report writer?

To thrive as a Commission Clinical Evaluation Report Writer, you need a strong background in life sciences or healthcare, expertise in clinical research methodologies, and familiarity with regulatory requirements such as EU MDR and MEDDEV 2.7/1 guidelines. Proficiency in literature review databases, reference management tools (e.g., EndNote), and document management systems is typically required. Exceptional analytical thinking, attention to detail, and effective written communication skills help set candidates apart in this role. These skills ensure the production of thorough, compliant, and scientifically sound reports essential for regulatory submissions and patient safety.

What are the primary challenges faced by a commission clinical evaluation report writer when gathering and analyzing clinical data from diverse sources?

One of the main challenges for a Commission Clinical Evaluation Report Writer is consolidating clinical data from various studies, which often differ in methodology, quality, and reporting standards. Ensuring that all relevant data is accurately synthesized while maintaining regulatory compliance requires attention to detail and strong critical analysis skills. Additionally, collaborating with cross-functional teams such as medical experts and regulatory affairs professionals is essential to verify findings and ensure the report meets both scientific and regulatory requirements. Balancing tight deadlines and evolving guidelines can also be demanding, but effective communication and organizational skills can help mitigate these challenges.

What is the difference between Commission Clinical Evaluation Report Writer vs Medical Device Regulatory Affairs Specialist?

AspectCommission Clinical Evaluation Report WriterMedical Device Regulatory Affairs Specialist
CredentialsMedical or scientific background, certifications in clinical evaluationRegulatory certifications, such as RAC or RAPS
Work EnvironmentHealthcare, medical device companies, clinical research settingsRegulatory agencies, medical device companies, compliance departments
Industry UsagePreparing clinical evaluation reports for medical device approvalEnsuring regulatory compliance and submissions for medical devices

The Commission Clinical Evaluation Report Writer focuses on creating detailed clinical evaluation reports for medical device approval, requiring clinical and medical expertise. In contrast, the Medical Device Regulatory Affairs Specialist handles broader regulatory compliance, including submissions and documentation. Both roles are essential in the medical device industry but differ in scope and primary responsibilities.

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Commission Clinical Evaluation Report Writer jobs near you
Infographic showing various Commission 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.

Epic Cogito Developer / Report Writer -Senior

University of Vermont Health

South Burlington, VT • On-site

$43.71 - $65.57/hr

Full-time

Re-posted 9 hours ago

Job description

Job Summary:
The Epic Cogito Developer / Report Writer designs, builds, and maintains reports, dashboards, and data extracts within the Epic Cogito reporting environment at UVM Health. This role deploys new SlicerDicer data models, performs impact analyses for Epic upgrades, and executes remediations to ensure reporting continuity. The Developer works alongside data analysts to understand stakeholder needs and delivers appropriate solutions using Epic tools, including direct interaction with stakeholders to further understand and refine requirements. The Developer collaborates closely with the Epic IT team, analysts, and clinical informatics staff.
Education:
• Bachelor's degree in Health Informatics, Computer Science, Data Science, or related field required.
• Epic Cogito Proficiency certification required or to be achieved within 120 days of hire; additional Cogito build certifications preferred.
Experience:
• 3+ years of experience with Epic Cogito reporting tools including Clarity, Caboodle, and Radar.
• Experience developing production Epic reports, dashboards, and SlicerDicer configurations.
• Experience deploying SlicerDicer data models and performing upgrade impact analyses and remediations.
• Experience in a healthcare setting.
• Working knowledge of SQL.
• Experience working in agile product delivery preferred.

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