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Cer Writer Jobs in Minnesota (NOW HIRING)

TESSCO

Customer Service Representative

Eden Prairie, MN · On-site

$55K - $65K/yr

The CER will focus on accurate order entry for all accounts in an assigned territory. Along with ... Excellent verbal and written communication skills * Must be organized and able to manage time ...

LivaNova

Regulatory & Clinical Specialist

Minneapolis, MN · 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 ...

Brooksource

Quality Technician

Minneapolis, MN · On-site

$52K - $63K/yr

May be required to work in a Controlled Environment Room (CER) as needed. * Effective written and verbal communication skills * Ability to work in a fast-paced environment while managing multiple ...

Laborie

Clinical Project Manager

Minnetonka, MN

$130K - $135K/yr

Therapeutic/intervention experience in urogynecology, gastroenterology, and/or OB/GYN. * Experience with medical devices CER, PMS, PMCF, PSUR medical writing. * Speak fluent English, excellent verbal ...

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$13

$37

$56

How much do cer writer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for cer writer in Minnesota is $37.84, according to ZipRecruiter salary data. Most workers in this role earn between $25.67 and $47.79 per hour, depending on experience, location, and employer.

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 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 popular job titles related to Cer Writer jobs in Minnesota? For Cer Writer jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Cer Writer jobs in Minnesota look for? The top searched job categories for Cer Writer jobs in Minnesota are:
What cities in Minnesota are hiring for Cer Writer jobs? Cities in Minnesota with the most Cer Writer job openings:
Cer Writer jobs near you
Infographic showing various Cer Writer job openings in Minnesota as of August 2026, with employment types broken down into 82% Full Time, 14% Part Time, and 4% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $78,709 per year, or $37.8 per hour.

Medical Writer

Three Point Solutions, Inc.

Maple Grove, MN • On-site

Full-time

Re-posted 5 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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