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Freelance Union Writer Jobs (NOW HIRING)

Fox

Senior Union Payroll Associate

New York, NY

$35.50 - $41.35/hr

... union freelance employees. The Senior Union Payroll Associate coordinates, validates, and ... Excellent verbal and written communication skills * Excellent judgment, analytical, and problem ...

Jobgether

In this freelance remote position, you will help train and evaluate AI models by reviewing vehicle ... High attention to detail and ability to follow structured written and visual guidelines.

Integrate

WLKY-TV Writer/Producer Intern

Louisville, KY · On-site

$20 - $25/hr

... through paid work, freelance projects, volunteering, self-directed learning, or other ... S viewers; newspapers such as the Houston Chronicle, San Francisco Chronicle and Times Union ...

Vox Media, LLC

Senior Video Producer

New York, NY · On-site

Manage and mentor freelance editors and designers, assigning work, giving creative feedback, and ... This role is a part of the Vox Media Union, represented by the Writers Guild of America, East OUR ...

Vox Media, LLC

Senior Video Producer

New York, NY · On-site +1

Manage and mentor freelance editors and designers, assigning work, giving creative feedback, and ... This role is a part of the Vox Media Union, represented by the Writers Guild of America, East OUR ...

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How much do freelance union writer jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for freelance union 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.
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Freelance Union Writer jobs near you
Medical Writer

Medical Writer

Three Point Solutions, Inc.

Maple Grove, MN • On-site

Full-time

Posted 3 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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