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Clinical Evaluation Report Writer Jobs (NOW HIRING)

Frontage Laboratories

Report Writer

Chicago, IL · On-site

$21.63 - $25.97/hr

... associated with the evaluation of the safety and/or toxicity of various materials (e.g ... Generating, formatting, and, reviewing pre-clinical main study reports and sub-reports.

St. Barnabas

Report Writer

Bronx, NY · On-site

Reports can be clinical or non-clinical in nature providing insight into clinical workflows ... The report writer will be responsible for developing specifications for, and writing individual ...

St Barnabas Hospital

Report Writer

Bronx, NY · On-site

Reports can be clinical or non-clinical in nature providing insight into clinical workflows ... The report writer will be responsible for developing specifications for, and writing individual ...

Abbott Laboratories

$90 - $180/hr

## Senior Project Manager/Clinical Evaluation Reporting (on-site)Candidatar-selocations: United States ... Report, and SSCP). As such, this person has oversight of internal and external CER Medical Writers ...

Jaca

The Clarity Report Writer- Clinical Applications utilizes multiple EHR systems in building reports required by the organization. The Clarity Report Writer- Clinical Applications assists in the ...

Alpha Consulting Corp.

Technical Report Writer

Alpha Consulting Corp. is seeking a Technical Report Writer to join their ITC-App/Dev Business ... Alpha Consulting Corp. has been exceeding expectations in the IT, pharmaceutical, and clinical ...

Miller Cooper

Super Set Report Writer

Winter Park, FL · Remote

NQS builds and supports clinical registry platforms serving trauma, burn, and emergency general ... NQS is seeking a talented and motivated Super Set Report Writer to join their innovative and ...

Abbott

Medical Writer IV

Abbott, TX · On-site +1

$65 - $68/hr

Writes and contributes to Clinical Evaluation reporting deliverables including Clinical Evaluation Plans/Reports, SSCPs, Regulatory Responses and other related documentation. * Evaluates and ...

Abbott

$65 - $68/hr

Daily activities are related to authoring Clinical Evaluation Reporting documents for the Vascular products. Experience in clinical study management and design, medical, or scientific writing, and/or ...

Miller Cooper

Super Set Report Writer

Winter Park, FL · On-site

$80K - $100K/yr

NQS builds and supports clinical registry platforms serving trauma, burn, and emergency general ... NQS is seeking a talented and motivated Super Set Report Writer to join their innovative and ...

Miller Cooper

Super Set Report Writer

Winter Park, FL · On-site

$80 - $100/hr

NQS builds and supports clinical registry platforms serving trauma, burn, and emergency general ... NQS is seeking a talented and motivated Super Set Report Writer to join their innovative and ...

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Clinical Evaluation Report Writer information

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

As of Sep 6, 2026, the average yearly pay for 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 clinical evaluation report writer?

A Clinical Evaluation Report (CER) Writer is responsible for preparing clinical evaluation reports required for medical device regulatory submissions. They analyze clinical data, review scientific literature, and ensure compliance with regulations like EU MDR and FDA guidelines. Their role involves collaborating with regulatory, clinical, and engineering teams to present accurate clinical evidence supporting a device’s safety and performance. Strong writing skills, regulatory knowledge, and an understanding of medical and scientific principles are essential for this role.

What does a typical workday look like for a clinical evaluation report writer?

A typical day for a Clinical Evaluation Report Writer involves reviewing scientific literature, analyzing clinical data, and drafting or updating Clinical Evaluation Reports (CERs) in compliance with regulatory standards. You will often work closely with regulatory affairs, clinical, and quality assurance teams to ensure the report meets submission requirements and addresses feedback from notified bodies. The role also includes conducting gap analyses, maintaining documentation, and staying up to date with relevant clinical guidelines. While the work is largely independent, frequent collaboration and clear communication with other departments are essential for success.

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

To thrive as a Clinical Evaluation Report Writer, you need a solid understanding of clinical research, regulatory requirements (such as MDR or IVDR), and scientific writing, typically supported by a degree in life sciences or a related field. Familiarity with literature review databases, referencing software (e.g., EndNote), and document management systems is crucial. Strong attention to detail, analytical thinking, and effective communication skills help you excel in collaborating with cross-functional teams and interpreting complex data. These competencies ensure that your reports are accurate, compliant, and contribute positively to the approval and ongoing monitoring of medical devices.

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Clinical Evaluation Report Writer jobs near you
Infographic showing various 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.

Report Writer

Frontage Laboratories

Chicago, IL • On-site

$21.63 - $25.97/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Job description

Report Writer

 

Title: Report Writer

Location: Chicago, IL, onsite

Reports to: Technical Report Supervisor

 

Full-time

 

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.


Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products.


Position/Job Summary: 

This position supports toxicologists in their preparation and presentation of reports, protocols or other documents associated with the evaluation of the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). The Report Writer prepares documents from information provided by personnel and/or subcontractors to be submitted to Study Sponsors. In addition to preparation of text, this position requires tabulation and summarization of data as well as some interpretation of results. Writers receive assignments from Study Directors and Management and are supervised by the Technical Writing Supervisor.


Roles & Responsibilities:


  • Generating, formatting, and, reviewing pre-clinical main study reports and sub-reports.
  • Coordinating and facilitating the compilation of report information from the Frontage study team (e.g., Study Directors, Study Supervisors, Management, and Quality Assurance personnel), Principal Investigators, and Contributing Scientists. 
  • Maintain consistent formatting across all Sponsor-facing documents by adhering to current style guidelines. 
  • Set up and troubleshoot table template generation for data outputs as well as quality check outputs for formatting/data errors.
  • Compile, organize, and present collected study data in a logical manner within summary and appendix sections of reports/sub-reports, as well as appropriately creating/linking in-text references to appended data.
  • Maintaining technical information in both electronic and paper formats. 
  • Generating new documents from pre-established template files following pre-established guidelines in their implementation and maintenance, or creating/maintaining new templates as needed. 
  • Tracking the preparation of report or other documents (e.g., protocols, study specific procedures) as well as the progress of study data as it is prepared for reports.
  • Maintaining open lines of communication within the reporting writing team, Study Directors, Quality Assurance, and Management regarding the status of reports/documents and data processing. 
  • Identifying and resolving problems related to the production of reports and other documents. 
  • Maintaining an understanding of pertinent governmental regulations (e.g., FDA, EPA, OECD, ICH, etc.), data handling best practices, and Sponsor guidelines.
  • Delivering assignments on time and adjusting regular business hours to accommodate deadlines. 


Education, Experience & Skills Required:

 

  • Must have a minimum of a BS/BA degree in a science/related discipline or prior experience that contributes directly and significantly to the individual’s technical writing competence. 
  • Experience with electronic document management; proficiency in Microsoft Word (general operation/document formatting) and Excel required.
  • Familiarity with Adobe Acrobat and Photoshop, or equivalent, for report compilation and finalization processes preferred.
  • Must possess strong organizational, grammatical, editorial/proofreading, reading comprehension, and critical thinking skills.
  • Must be able self-start independent work, cooperatively interact with study team members toward common goals, and to work on multiple projects concurrently. 
  • Must possess excellent communication skills to effectively interact with other personnel.
  • Familiarity with adherence to protocol/SOP-specified parameters preferred.


Salary: $21.63-$25.97/hour


Benefits:

  • 401k Employer Match with immediate vesting
  • Vision Insurance 
  • Medical and Dental Insurance with multiple coverage options
  • FSA (Medical, Dependent Care, and Commuter)
  • Short Term Disability
  • Long Term Disability 
  • Life Insurance
  • Generous Paid Holidays and PTO 

 

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.