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Freelance Pfizer Medical Writer Jobs (NOW HIRING)

Principal Medical Writer

Cranbury, NJ · On-site

$95K - $105K/yr

Assign tasks to internal writers and freelancers, managing workflow and reassigning tasks as needed ... Medical Event Attendance: * Attend live events such as consensus meetings and professional ...

Review/revise medical writers and freelance writers' work as necessary * Participate in brainstorming sessions and strategic publications planning meetings to aid in strategy/goals * Attend advisory ...

Review/revise medical writers and freelance writers' work as necessary * Participate in brainstorming sessions and strategic publications planning meetings to aid in strategy/goals * Attend advisory ...

... Pfizer Field Medical colleagues (d) Demonstrate expertise in communication across multiple channels, including, but not limited to, live and virtual presentations in small or large settings, written ...

Principal Validation Engineer

Andover, MA · On-site

$124K - $207K/yr

Effective written and verbal communication skills * Strong interpersonal skills and the ability to ... medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S.

Deep understanding of I&I drug development, protocol writing, study conduct, data analysis, and ... medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S.

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How much do freelance pfizer medical writer jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for freelance pfizer medical 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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Infographic showing various Freelance Pfizer Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $48,412 per year, or $23.3 per hour.

Full-time

Re-posted 7 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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