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Cer Writer Jobs in Georgia (NOW HIRING)

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 ...

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 ...

BrandSmart

Customer Service Representative

Kennesaw, GA

$14.75 - $20/hr

The CER must be able to communicate with multiple departments, buyers, management, and retail store ... Ability to read and write fluently in English (or another language as may be required) sufficiently ...

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · Remote

$85K - $95K/yr

Experience writing Clinical Evaluation Plans and Reports (CEP, CER, respectively) to support EU MDD and MDR requirements. * Expertise in conducting focused literature searches on PubMed, Embase ...

Aaron's

Customer Experience Representative

Atlanta, GA · On-site

$15.75 - $21.25/hr

The CER must be able to communicate with multiple departments, buyers, management, and retail store ... Ability to read and write fluently in English (or another language as may be required) sufficiently ...

Aaron's

Part-Time Customer Service Team Member

Kennesaw, GA · On-site

$14.75 - $20/hr

The CER must be able to communicate with multiple departments, buyers, management, and retail store ... Ability to read and write fluently in English (or another language as may be required) sufficiently ...

Aaron's

Customer Experience Repr

Stockbridge, GA · On-site

$12/hr

Summary: The Customer Experience Representative (CER) will act as a liaison between various ... Ability to read and write fluently in English (or another language as may be required) sufficiently ...

Aaron's

Customer Service Representative

Kennesaw, GA · On-site

$14.75 - $20/hr

The CER must be able to communicate with multiple departments, buyers, management, and retail store ... Ability to read and write fluently in English (or another language as may be required) sufficiently ...

Intertek

Building Enclosure Project Manager

Kennesaw, GA · On-site

$83K - $113K/yr

Prepare professionally written technical reports * Prepare sketches and/or mark-up details using Bluebeam or hand-written techniques This position outline is a general guideline and does not ...

TERRACON

CMT Engineering Technician III

Macon, GA · On-site

Tabulate, prepare, and submit data and observation in the form of written and digital reports as ... Successful completion of related internal safety cer About Us Terracon is a 100 percent employee ...

TERRACON

CMT Engineering Technician III

Macon, GA

Tabulate, prepare, and submit data and observation in the form of written and digital reports as ... Successful completion of related internal safety cer * Performs testing, observation, and ...

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Cer Writer information

See Georgia salary details

$11

$32

$48

How much do cer writer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for cer writer in Georgia is $32.62, according to ZipRecruiter salary data. Most workers in this role earn between $22.12 and $41.20 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.

What are popular job titles related to Cer Writer jobs in Georgia?

For Cer Writer jobs in Georgia, the most frequently searched job titles are:

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

The top searched job categories for Cer Writer jobs in Georgia are:

Cer Writer jobs near you
Infographic showing various Cer Writer job openings in Georgia as of August 2026, with employment types broken down into 55% Full Time, 35% Part Time, 7% Contract, and 3% Nights. Highlights an 54% Physical, 3% Hybrid, and 43% Remote job distribution, with an average salary of $67,858 per year, or $32.6 per hour.

Senior Medical Writer

Artivion

Kennesaw, GA • On-site

Full-time

Re-posted 22 days ago

Artivion rating

8.7

Company rating: 8.7 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

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.

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