ZipRecruiter

Log In

1

Clinical Report Writer Jobs (NOW HIRING)

Natera

Manager, Clinical Trials

OR · On-site +1

... clinical report preparation, as required * Collaborate with Clinical Data Management group to ... Strong interpersonal skills and communication skills (both written and oral) * Strong leadership ...

Vaxcyte

Director, Clinical Medical Writing

San Carlos, CA · On-site +1

$221K - $258K/yr

... reports, etc.), providing guidance on scientific and technical requirements for regulatory ... Experience as lead writer for key documents included in major US and/or international regulatory ...

Merck & Co.

May manage direct reports including workload, professional development, and performance management ... writers and/or cross-functional team members.Ability to critically evaluate and interpret clinical ...

Worldwide Clinical Trials

Clinical Scientist

Durham, NC · On-site +1

Review data-driven sections of regulatory and clinical reporting documents (e.g., CSRs, INDs, NDAs/BLAs, annual reports, IBs, etc.). * Provide scientific writing support, including patient narratives ...

previous page

Showing results 41-60

All JobsEducation JobsBusiness Education JobsScientific Writer JobsClinical Report Writer Jobs

Clinical Report Writer information

See salary details

$42K

$78.9K

$136K

How much do clinical report writer jobs pay per year?

As of Sep 8, 2026, the average yearly pay for clinical report writer in the United States is $78,865.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $102,000.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Report Writer vs Medical Writer?

AspectClinical Report WriterMedical Writer
CredentialsOften requires a background in healthcare, life sciences, or related fields; certifications like RAC or CCR may be preferredTypically holds degrees in life sciences, healthcare, or communications; certifications like AMWA or EMWA are common
Work EnvironmentWorks in clinical research settings, pharmaceutical companies, or healthcare organizationsWorks in publishing, pharmaceutical, biotech, or healthcare communication firms
Industry UsageUsed primarily in clinical trial documentation and regulatory submissionsUsed for scientific publications, marketing materials, and regulatory documents

While both roles involve scientific writing, Clinical Report Writers focus on clinical trial documentation and regulatory reports, whereas Medical Writers produce a broader range of medical content including publications and marketing materials. The roles often overlap but serve different primary purposes within the healthcare and pharmaceutical industries.

What does a clinical report writer do?

A clinical report writer creates detailed documents that summarize clinical trial data, research findings, and medical information for regulatory submissions, publications, or internal use. They often use specialized software and must ensure accuracy, clarity, and compliance with industry standards. Strong writing skills and knowledge of medical terminology are essential for this role.

What cities are hiring for Clinical Report Writer jobs?

Cities with the most Clinical Report Writer job openings:

What states have the most Clinical Report Writer jobs?

States with the most job openings for Clinical Report Writer jobs include:

What are popular job titles related to Clinical Report Writer jobs?

For Clinical Report Writer jobs, the most frequently searched job titles are:

Infographic showing various Clinical Report Writer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,865 per year, or $37.9 per hour.

Medical Writer

Maple Grove, MN • On-site

Three Point Solutions, Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Three Point Solutions, Inc.external

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