ZipRecruiter

Log In

1

Cer Writer Jobs (NOW HIRING)

CryoLife

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 ...

Merit

Senior Medical Writer

COMPETENCIES Medical/technical writing skills CER protocol and report development/writing Medical literature research skills Computer skills Interpersonal/verbal/written communication skills Project ...

CER MANAGEMENT GROUP LLC

Mig Welder

Anderson, SC · On-site

$16 - $19.75/hr

Apply skills to carry out instructions furnished in written and oral form * Satisfactorily perform ... Company Description CER MANAGEMENT GROUP Has a team specialist in the process for recruitment and ...

Palmer Trucks

Service Writer I

Effingham, IL · On-site

SERVICE WRITER Reports To: Service Manager Summary The primary function of the Service Writer is ensure customers are greeted openly and friendly and to provide extra mile customer service. The ...

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

... CER) and associated documentation. Specifically contributes to the planning, literature review and ... Writes and or edits clinical study documentation, including clinical investigational plans ...

Getinge

Medical Writer (Remote, US)

Boston, MA · On-site +1

... CER) and associated documentation. Specifically contributes to the planning, literature review and ... Writes and or edits clinical study documentation, including clinical investigational plans ...

Abbott Laboratories

$90 - $180/hr

Scientific / Medical writing experience is required. In addition, the CER PM will interact cross-functionally with various personnel to identify and obtain relevant documentation including data on ...

CER MANAGEMENT GROUP LLC

Mig Welder

Greenville, SC · On-site

$17.50 - $21.50/hr

Apply skills to carry out instructions furnished in written and oral form * Satisfactorily perform ... Company Description CER MANAGEMENT GROUP Has a team specialist in the process for recruitment and ...

previous pagenext page

Showing results 21-40

All JobsEducation JobsBusiness Education JobsTechnical Writer JobsCer Writer Jobs

Cer Writer information

See salary details

$14

$38

$57

How much do cer writer jobs pay per hour?

As of Aug 22, 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.

More about Cer Writer jobs

What cities are hiring for Cer Writer jobs?

Cities with the most Cer Writer job openings:

What are the most commonly searched types of Cer Writer jobs?

The most popular types of Cer Writer jobs are:

What states have the most Cer Writer jobs?

States with the most job openings for Cer Writer jobs include:

What job categories do people searching Cer Writer jobs look for?

The top searched job categories for Cer Writer jobs are:

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.

Senior Medical Writer

CryoLife

Kennesaw, GA • On-site

Full-time

Re-posted 22 days ago

Job description

Company Overview
Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in treating patients with aortic diseases. Artivion's four major groups of products include: aortic stent grafts, surgical sealants, On-X mechanical heart valves, and implantable cardiac and vascular human tissues. Artivion has over 1,600 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, www.artivion.com.
Responsibilities:
  • Support product line compliance to US and International regulations and standards as applicable
  • Writing clinical regulatory documents including annual reports, study summaries, and other study rationales.
  • Support clinical requirements for regulatory submissions and maintenance.
  • Coordinating company deliverables such as but not limited to the CEP, CER, PMCF activities and SSCP process for MDR compliance
  • Collaborate with other departments to work as a team to accomplish tasks
  • Effectively communicate timelines and hold team members accountable to agreed upon timelines required for project dates.
  • Conduct literature reviews and write research summaries related to product line.
  • Support preparation of product IFUs and assist with labeling and labeling changes (including receipt of applicable translations).
  • Effectively present and share clinical data.
  • Develop and maintain any applicable clinical research databases as necessary.
  • Generate interim analysis, investigator meeting slides, and final clinical study reports.
  • Communicate with physicians, vendors, and other medical experts.
  • Report on adverse events, complaints, and failures associated with the product line identified through the writing process
  • Coordinate the execution of peer-reviewed projects (publications, posters, abstracts) and marketing literature.
  • Oversee project timelines, budgets, budget change forms, accruals, and monthly reports associated with vendor supported projects
  • Generate clinical study documents including but not limited to: protocols, investigational plans, informed consent forms, handouts, SOPs, and status reports.
  • Liaison between Artivion, investigational sites, and CROs (as applicable) to coordinate and document final reports and publications.
  • Other assigned responsibilities (including previously identified tasks being performed at a higher level than one's current title).
  • Support the development of clinical regulatory documents to support product maintenance.

Qualifications:
  • Minimum 3-4 years' experience writing within the medical/biomedical industry.
  • BS or MS degree in biological science, epidemiology, engineering, statistics, or other science related field.
  • Knowledge of regulatory requirements relative to medical devices including Clinical Evaluation Reports and Post Market Requirements
  • Ability to write and edit quality medical abstracts, white papers, manuscripts, and other educational materials.
  • Experience with literature searches and analysis.
  • Demonstrate computer skills (spreadsheet, relational databases).
  • Excellent written and oral communication skills.
  • Excellent interpersonal skills.
  • Ability to manage multiple projects.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Apply