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Remote Cer Writer Jobs (NOW HIRING)

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 ...

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Chicago, IL · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Denver, CO · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Austin, TX · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Boston, MA · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Phoenix, AZ · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Houston, TX · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Dallas, TX · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

LivaNova

Regulatory & Clinical Specialist

Charlotte, NC · Remote

$85K - $95K/yr

Skills and Experience * Experience writing Clinical Evaluation Plans and Reports (CEP, CER ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

The Pennsylvania State University

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Past success in writing white papers or report Preferred skills/experience areas include: * Model ...

Software People, Inc.

Cerner Analyst with HL7

Cayce, SC · Remote

Mostly remote Role is remote aside from occasional in-person site visits which can be expected to ... Provide knowledge and understanding of DCWs, maintenance, and Discern rules writing for specific ...

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Remote Cer Writer information

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$35

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How much do remote cer writer jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for remote cer writer in the United States is $35.11, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $50.96 per hour, depending on experience, location, and employer.

What is a Remote CER Writer?

A Remote CER Writer is a professional who specializes in creating Clinical Evaluation Reports (CERs) for medical devices, working from a remote location. CER Writers gather, analyze, and synthesize clinical data to demonstrate the safety and performance of medical devices as required by regulatory authorities like the European Medicines Agency (EMA) or FDA. They collaborate with regulatory teams, subject matter experts, and sometimes clinical researchers to ensure all documentation meets strict compliance and quality standards. Working remotely allows these professionals to perform their tasks from anywhere, using digital tools to communicate and manage documentation.

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

AspectRemote Cer WriterRemote Medical Writer
Required CredentialsCertification in medical writing or related fields, sometimes specific to certification bodiesMedical or life sciences degree, often with certification in medical writing
Work EnvironmentHome-based, flexible schedules, often project-basedHome-based, with collaboration in teams, deadlines for regulatory documents
Industry UsagePharmaceutical, healthcare, regulatory agenciesPharmaceutical, biotech, medical communications
Common Search/ComparisonRemote Cer Writer vs Remote Medical Writer

Remote Cer Writers focus on creating clinical and regulatory documentation for healthcare and pharmaceutical companies, often requiring certification in medical writing. Remote Medical Writers also produce scientific content but may work on a broader range of medical communications, including marketing and educational materials. Both roles are home-based, require relevant credentials, and serve the healthcare industry, but their specific focus and types of documents differ.

What are some common challenges faced by Remote CER Writers, and how can they be effectively managed?

Remote CER Writers often encounter challenges such as coordinating with global teams across different time zones, managing large volumes of scientific literature, and ensuring timely access to subject matter experts for clinical evaluation report inputs. Effective communication tools, well-organized project management systems, and proactive scheduling of virtual meetings can help mitigate these challenges. Building strong relationships with regulatory, clinical, and quality teams also facilitates smoother collaboration and ensures the CER meets stringent regulatory requirements.

What are the key skills and qualifications needed to thrive as a Remote CER Writer, and why are they important?

To thrive as a Remote CER Writer, you need a strong background in scientific writing, clinical research, and regulatory knowledge, often supported by a degree in life sciences or related fields. Familiarity with regulatory guidelines (such as MDR, MEDDEV 2.7/1), literature review databases, and document management systems is essential. Attention to detail, strong organizational skills, and clear communication are vital soft skills for producing high-quality Clinical Evaluation Reports (CERs) remotely. These skills ensure regulatory compliance, clarity, and accuracy in documentation, which are critical for successful medical device approvals.
More about Remote Cer Writer jobs
What cities are hiring for Remote Cer Writer jobs? Cities with the most Remote 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 Remote Cer Writer jobs? States with the most job openings for Remote Cer Writer jobs include:
What job categories do people searching Remote Cer Writer jobs look for? The top searched job categories for Remote Cer Writer jobs are:
Remote Cer Writer jobs near you
Infographic showing various Remote Cer Writer job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $73,039 per year, or $35.1 per hour.

Medical Writer (Remote, US)

Getinge

Boston, MA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago

Getinge rating

9.3

Company rating: 9.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

10th of 487 rated machine equipment manufacturers

Job description

With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
Job Overview
Responsible for the generation and development of documents relating to clinical evaluations and clinical investigations.
This position is hybrid or fully remote in the US preferably on EST zone.
This is a fixed term position with direct hire with Getinge with a high potential to convert to regular hire.
Job Responsibilities and Essential Duties
  • Serves as a clinical evaluation lead and participates within the clinical evaluation team for the development and generation of Clinical Evaluation Reports (CER) and associated documentation. Specifically contributes to the planning, literature review and the identification, appraisal and analysis of clinical data related to the evaluation in accordance to MEDDEV 2.7/1 Revision 4 and in alignment with EU MDR. Contributes to the Summary of Safety and Clinical Performance in alignment with EU MDR.
  • Serves as point and participates in the Post-Market Clinical Follow-up (PMCF) team. Specifically contributes to the literature review and the identification and analysis of clinical data related to the PMCF evaluation.
  • Performs comprehensive systematic, documented literature reviews using various search engines in order to support the Clinical Evaluation, Post-market Clinical Follow-Up, awareness of current State of the Art as well as protocol development and any ad hoc reports required. (20%)
  • Analyzes available clinical evidence (data held by the manufacturer, published literature) to assist the Clinical Affairs team with clinical development strategy.
  • Writes and or edits clinical study documentation, including clinical investigational plans/protocols, Investigator's Brochures, Periodic reports, Clinical Investigational Reports/Clinical Study Reports. Ensure high quality study documentation that is submission-ready for various regulatory agency and external distribution.
  • Serves as a subject matter expert on clinical aspects of Technical documentation.
  • Writes and/or supports the development of manuscripts relating to clinical study data or clinical evidence for submission to peer-reviewed medical journals. Works with medical professionals to ensure alignment with journal requirements for targeted manuscript submission.
  • Writes and/or contributes to abstracts and submissions of clinical data to various medical congresses or symposia. Work with medical professionals to ensure high quality submissions and data integrity.
  • Contributes to the development and optimization of Clinical Affairs SOPs.
  • Performs other non-routine duties as assigned.

Required Knowledge, Skills and Abilities
  • Bachelors Degree in a relevant scientific discipline, or equivalent combination of education and experience.
  • A minimum of 3 years medical writing experience. Direct experience working on clinical evaluations within the Medical Device industry a plus.
  • Medical writing certification a plus.
  • A high level attention to detail and the ability to own and drive accuracy.
  • Strong interpersonal and communication skills.
  • Excellent project management skills with the ability to deliver projects on timelines that support corporate and departmental goals and objectives.
  • Strong analytical and organizational skills as well as demonstrated ability to solve problems with innovative solutions
  • Outstanding oral and written communication skills.
  • Proficiency in using and navigating PubMed, Embase and other literature search engines. Experience in DistillerSR, EndNote and other literature review tools a plus.
  • Strong working knowledge of regulations and guidance relating to Clinical Affairs, including EU MDR (2017/745), EU MDD (93/42/EEC), MEDDEV guidance, including 2.7/1 Revision 4 and 2.12/2 Revision 2, relevant MDCG guidance, ISO 14155, ICH guidance including E3 CSR, E6 (R3) GCP, and familiarity regulations/ guideline relating to Risk management (i.e. ISO 13485 and ISO14971)
  • Demonstrated ability to work independently and as part of a team.
  • Ability to interact with physicians in a professional manner.
  • Ability to prioritize tasks in a fast-paced environment. Ability to work under urgent deadlines and flexibility to accommodate fluctuating timelines.
  • Advanced skills using Microsoft Office products such as Outlook, Word, Excel and Power Point.
  • Travel requirements depending on projects.

Internal and External Contacts/Relationships
  • Internal Getinge teams such as Medical Affairs, Regulatory Affairs, Quality Engineering, Research & Development and Marketing, as needed.
  • External teams such as CROs, clinical vendors and key opinion leaders.

The base salary for the position is a minimum of $105,000 and a maximum of $115,000
#LI-JF1 #LI-remote
About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
  • Health, Dental, and Vision insurance benefits
  • 401k plan with company match
  • Paid Time Off
  • Wellness initiative & Health Assistance Resources
  • Life Insurance
  • Short and Long Term Disability Benefits
  • Health and Dependent Care Flexible Spending Accounts
  • Commuter Benefits
  • Parental and Caregiver Leave
  • Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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About Getinge

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dr Wayne, NJ, US

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