ZipRecruiter

Log In

1

Freelance Cme Writer Jobs (NOW HIRING)

Everyday Health - Professional

Review content developed by other medical writers and freelancers, and provide guidance and/or ... Prefer experience in developing CME/CE activities supported by pharmaceutical companies and ...

Everyday Health - Professional

Review content developed by other medical writers and freelancers, and provide guidance and/or ... Prefer experience in developing CME/CE activities supported by pharmaceutical companies and ...

Advocate Health

CRNA - Davie Medical Center

Advance, NC · On-site

$12K/mo

Enjoy 10-hour shifts, with ample freelance opportunities! * CME Reimbursement: Receive up to $2,500 ... Strong verbal and written communication skills to effectively collaborate with diverse clinical ...

MJH Life Sciences

Event Manager

Cranbury, NJ · On-site

On site: event manager(s), coordinators, temporary, and freelance staff. & RESPONSIBILITIES ... Initiate, analyze and compare written quotes from vendors such as venues, audio visual ...

All JobsCme Writer JobsFreelance Cme Writer Jobs

Freelance Cme Writer information

See salary details

$7

$23

$32

How much do freelance cme writer jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for freelance cme writer in the United States is $23.27, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $26.20 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Cme Writer jobs? The most popular types of Cme Writer jobs are:
Freelance Cme Writer jobs near you
Medical Writer

Medical Writer

Three Point Solutions, Inc.

Maple Grove, MN • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

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.

#ZR

Apply