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Contract Medical Writer Clinical Research Jobs (NOW HIRING)

Trident Consulting

Medical Writer

Irvine, CA · On-site

$40 - $44/hr

Contract (W2) Pay Rate: $40/hr - $44/hr on W2 Duration: 6 Months About the Role We are seeking a ... This role will collaborate with Clinical, Regulatory, and R&D teams to develop high-quality ...

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Clear Point Consultants

Medical Writer

Boston, MA · On-site

$55 - $70/hr

... month contract | Potential for extension or conversion 💰 $55-$70/hour ⏰ 40 hours/week We are ... Approximately 4+ years of relevant experience in medical writing, clinical research, drug ...

Solventum

Medical Writer - Clinical Compliance

$124K - $170K/yr

Medical Writer - Clinical Compliance(Solventum) 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of ...

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How much do contract medical writer clinical research jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for contract medical writer clinical research 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.

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Medical Writer

Three Point Solutions, Inc.

Maple Grove, MN • On-site

Full-time

Re-posted 21 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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