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Cer Medical 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 ...

Abbott Laboratories

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 ...

Artivion

Senior Medical Writer

Kennesaw, GA

Coordinating company deliverables such as but not limited to the CEP, CER, PMCF activities and SSCP ... Ability to write and edit quality medical abstracts, white papers, manuscripts, and other ...

CryoLife

Senior Medical Writer

Kennesaw, GA · On-site

Coordinating company deliverables such as but not limited to the CEP, CER, PMCF activities and SSCP ... Ability to write and edit quality medical abstracts, white papers, manuscripts, and other ...

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 contributes to abstracts and submissions of clinical data to various medical ...

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 contributes to abstracts and submissions of clinical data to various medical ...

Edwards Lifesciences

$108K - $153K/yr

Experience with clinical evaluation report (CER) development under MEDDEV 2.7/1 REV. 4 and/or the ... medical writing * Good leadership skills and ability to influence change * Strict attention to ...

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Cer Medical Writer information

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$78

How much do cer medical writer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for cer medical writer in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

What is a CER Medical Writer?

A CER Medical Writer is a professional who specializes in creating Clinical Evaluation Reports (CERs) for medical devices. These reports are essential documents required by regulatory authorities, such as the European Medicines Agency (EMA) and the FDA, to demonstrate the safety and performance of medical devices. CER Medical Writers gather, analyze, and interpret clinical data, ensuring that the documentation meets stringent regulatory standards. Their work supports manufacturers in obtaining and maintaining regulatory approval for medical devices.

What are the key skills and qualifications needed to thrive as a CER Medical Writer?

To thrive as a CER (Clinical Evaluation Report) Medical Writer, you need a strong background in life sciences or medicine, excellent scientific writing skills, and familiarity with regulatory requirements such as MDR and MEDDEV 2.7/1. Proficiency in literature search databases (e.g., PubMed), reference management tools, and document management systems is typically required, along with an understanding of clinical research methodologies. Attention to detail, critical thinking, and effective communication are valuable soft skills for distilling complex data and collaborating with cross-functional teams. These abilities ensure the creation of accurate, compliant CERs that support regulatory submissions and product safety.

What are the typical collaboration dynamics between a CER Medical Writer and cross-functional teams?

CER Medical Writers frequently collaborate with clinical, regulatory, and quality assurance teams to develop Clinical Evaluation Reports (CERs) that meet regulatory standards. This role often involves participating in meetings to gather input, reviewing clinical data, and incorporating feedback from subject matter experts. Effective communication and the ability to translate complex scientific information for diverse audiences are essential. Building strong relationships with colleagues can greatly streamline the report development process and ensure compliance with evolving regulations.

What is the difference between Cer Medical Writer vs Medical Writer?

AspectCer Medical WriterMedical Writer
CredentialsOften requires certification in medical writing or related fieldsMay or may not have specific certifications, but typically has a degree in life sciences or related fields
Work EnvironmentPharmaceutical, biotech, or medical device companies, regulatory agenciesHealthcare, publishing, or consulting firms, regulatory bodies
Industry UsagePrimarily in regulated industries requiring compliance with standards like ISO 13485 or FDABroader healthcare and scientific communication sectors

While both roles involve creating scientific and medical content, Cer Medical Writers specialize in regulatory documentation for medical devices, often requiring specific certifications and compliance knowledge. Medical Writers have a broader scope, including educational materials, journal articles, and marketing content, with less emphasis on regulatory certification.

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Cer Medical Writer jobs near you
Infographic showing various Cer Medical Writer job openings in the United States as of September 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Medical Writer

Maple Grove, MN • On-site

Three Point Solutions, Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Three Point Solutions, Inc.external

Full-time

Re-posted 9 days ago

Job description

Job Title: Medical Writer
Client: Medical Device Manufacturing Company
Duration: 12 Months
Location: Maple Grove, MN, 55311
**Mandatory- Must be US Citizen or Green Card Holder Only
Key Words:
  • CER (Clinical Evaluation Review/Report) Writing
  • MDR (Medical Device Regulations)
  • EU (European Union)
  • Literature Review (e.g., PubMed)

Responsibilities:
  • Write and review scientific manuscripts, congress abstracts, and scientific meeting presentations aligned with journal and congress guidelines.
  • Prepare clinical content for study investigator meetings, interim data analyses, and other internal/external meetings related to clinical studies.
  • Create symposia (non-CME), speaker decks, post-meeting slide decks, topical slide decks, and other Professional Education modules as needed.
  • Collaborate extensively with internal medical leadership, clinical research scientists, clinical trial managers, medical affairs managers, statisticians, and other medical writers as part of publication teams.
  • Develop partnerships with study investigators, external authors, and interact externally with journals, conference organizers, and freelance/contract medical writers.
  • Ensure clinical data is represented accurately in published literature, slide sets, and other materials.
  • Lead and organize document production meetings and related activities.
  • Review documents related to clinical evidence for proper evaluation and presentation of data, methodology, and interpretation.

Required Qualifications:
  • Degree in Life Sciences (Advanced degree preferred).
  • Experience in Medical Device or Pharmaceutical Industry with a focus on Medical Writing or Clinical Research.
  • Extensive experience in writing, editing, and submitting publications to journals and congresses.

Preferred Qualifications:
  • 5-7 years of relevant experience.
  • Therapeutic area knowledge in peripheral interventions is desired.
  • Excellent written, analytical, verbal, and communication skills.
  • Ability to manage multiple projects independently and meet deliverables on time.
  • Capable of working effectively in a matrix environment.
  • Ability to develop strategic solutions to significant business issues.
  • Commitment to patient safety and product quality by adhering to the Quality Policy and documented quality processes and procedures.

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