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Cer Writer Jobs (NOW HIRING)

Abbott

Medical Writer IV

Abbott, TX · On-site +1

$65 - $68/hr

Medical Writer IV Location: Remote Duration: 12 Months Remote Summary: The Medical Writer on our ... Collaborates with team members and stakeholders in planning for and supporting CER related projects ...

Abbott

$65 - $68/hr

Medical Writer IV Location: Remote Duration: 12 Months Remote Summary: The Medical Writer on our ... Collaborates with team members and stakeholders in planning for and supporting CER related projects ...

Artivion

Senior Medical Writer

Kennesaw, GA · On-site

Writing clinical regulatory documents including annual reports, study summaries, and other study ... Coordinating company deliverables such as but not limited to the CEP, CER, PMCF activities and SSCP ...

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CER Writer information

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How much do cer writer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for cer writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is a Cer Writer?

A CER (Clinical Evaluation Report) Writer is responsible for preparing detailed reports that assess the safety and performance of medical devices. They analyze clinical data, regulatory requirements, and scientific literature to ensure compliance with regulations like the EU MDR. CER Writers collaborate with regulatory teams, medical experts, and researchers to compile and present findings in a clear and structured manner. Their work is essential for obtaining and maintaining medical device approvals in global markets.

What are the most common challenges faced by Cer Writers in their daily work?

One of the most common challenges for CER Writers is gathering and interpreting comprehensive clinical data from various sources while ensuring compliance with ever-evolving regulatory requirements. The role often involves collaborating with clinical, regulatory, and product development teams to fill information gaps and clarify technical details. Additionally, managing tight deadlines and adapting to changes in regulatory expectations can create pressure. However, strong organization and communication skills can help CER Writers overcome these challenges and deliver accurate, timely reports that are critical for medical device approval and market access.

What are the key skills and qualifications needed to thrive in the Cer Writer position, and why are they important?

To thrive as a CER Writer, you need a strong background in scientific writing, clinical research, and regulatory compliance, often supported by a degree in life sciences or pharmacy. Familiarity with relevant guidelines such as MEDDEV 2.7/1 and proficiency with literature databases and referencing tools like EndNote are crucial. Attention to detail, critical thinking, and effective communication are key soft skills for synthesizing data and collaborating with cross-functional teams. These skills ensure the development of high-quality Clinical Evaluation Reports that meet stringent regulatory standards and support product approvals.

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CER Writer jobs near you
Infographic showing various Cer Writer job openings in the United States as of August 2026, with employment types broken down into 56% Full Time, 41% Part Time, and 3% Contract. Highlights an 55% Physical, 2% Hybrid, and 43% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Medical Writer IV

Abbott

Abbott, TX • On-site, Remote

$65 - $68/hr

Contractor

Medical, Dental, Vision, Life, Retirement

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

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

175th of 543 rated manufacturers

Job description

Title: Medical Writer IV
Location: Remote
Duration: 12 Months
Remote
Summary:
The Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing expertise throughout the product development and life cycle process. 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 quality engineering/risk management and strong written and verbal communication skills are needed.
Responsibilities:
  • Writes and contributes to Clinical Evaluation reporting deliverables including Clinical Evaluation Plans/Reports, SSCPs, Regulatory Responses and other related documentation.
  • Evaluates and summarizes clinical evidence including data from sources such as clinical investigations, literature, post-market surveillance, risk, and post market clinical evaluations. Analyzes results in preparation for product applications and submissions.
  • Collaborates with team members and stakeholders in planning for and supporting CER related projects and processes.
  • Supports additional clinical, regulatory, quality and engineering related deliverable as assigned.
  • Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs, Clinical Science, Risk Management and Medical Affairs in completing clinical evaluation project related deliverables.
  • Maintains thorough knowledge of assigned products. Identifies appropriate sources of relevant data, interprets, evaluates, and incorporates information from various sources including literature, clinical data, and medical references.
  • Reviews IFUs, patient guides, Risk Management files, Clinical Evaluation Protocols, Clinical Evaluation Reports and Plans (CER/CEP), PMS Plan, PMCF Plans/Reports, SSCPs, physician training materials, ensuring alignment of risk information. Involved in responses to complex queries such as those issued by notified bodies and stakeholders.
  • Authors and contributes to necessary documents for regulatory submissions and communications, risk reviews, and other processes such as regulatory inquiries.
  • Ensures quality in all deliverables and documentation with attention to detail, consistency, and integrity of data. Responsible for compliance with applicable corporate and divisional policies and procedures. Ensures compliance to applicable regulations and guidance's (ISO13485, ISO14155, ISO14791, MEDDEV 2.7.1, MDR, and EU and FDA guidance documents) and applicable Abbott SOPs and DOPs.

Education:
  • 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 general technical writing experience required
  • Experience may include writing experience in a medical, pharmaceutical, medical device, clinical research, medical or research industry, or combination of these skills

Preferred:
  • Biomedical, sciences, medicine or similar health related discipline preferred
  • CER writing experience preferred
  • Excellent written and verbal communication skills
  • Experience with collaborative, cross-functional teams.
  • Excellent analytical skills and ability to manage complex tasks and manage time effectively
  • Proficient with Word, Excel, PowerPoint, Outlook, etc.

Consultants Eligible Benefits Upon Waiting Period:
  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High-Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
  • Published on 13 Aug 2026, 7:20 PM

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