2

Remote International Medical Writer Jobs (NOW HIRING)

Medical Writer (Remote)

OR · Remote

$85 - $90/hr

Medical Writer Contract Position - 6 months with potential extension Position Summary Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in ...

Senior Medical Writer (Remote) Arthrex, Inc. is a global medical device company and a leader in new ... This position will play a critical role in regulatory approval efforts for international markets.

Medical Writer

$78K - $102K/yr

Advance your medical writing career with purpose and impact. Work shouldn't just be something we do ... We welcome applications from candidates in the US and Ontario, Canada and support both remote ...

Remote Shift: Mon-Fri 9.00 AM-5.00 PM * We are seeking a skilled Medical Writer to develop high-quality clinical and regulatory documents in compliance with industry standards and regulatory ...

THE CONTRACT MEDICAL WRITER-PUBLICATIONS ROLE We are seeking an experienced Medical Writer to ... This role is remote and on an as-needed basis as determined by Sorcero project volume and the ideal ...

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

Fully Remote (U.S.) Industry: Pharmaceutical / Biotechnology Employment Type: Full-Time Salary ... Medical Writer to support clinical development and regulatory documentation activities within a ...

Sr. Medical Writer

Princeton, NJ · Remote

$116K - $137K/yr

Remote Employee Value Proposition: At Taiho Oncology, the compassion we practice for our patients ... The Senior Medical Writer, Medical Writing is accountable for the timely delivery of high quality ...

Remote and hybrid working options as standard * Continuous learning and professional development ... Job code: CPT407 Career opportunities Medical writing Role Publications Locations USA (Remote ...

HEOR Medical Writer

Whippany, NJ · On-site +1

$30 - $40/hr

Medical Writer - Clinical Content & Health Economics and Outcomes Research (HEOR), Clinical Content ... Remote Duration: 6 month contract with the potential for extension, based on performance Targeted ...

next page

Showing results 1-20

Remote International Medical Writer information

See salary details

$14

$38

$57

How much do remote international medical writer jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for remote international medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.
More about Remote International Medical Writer jobs
What cities are hiring for Remote International Medical Writer jobs? Cities with the most Remote International Medical Writer job openings:
What are the most commonly searched types of International Medical Writer jobs? The most popular types of International Medical Writer jobs are:
What states have the most Remote International Medical Writer jobs? States with the most job openings for Remote International Medical Writer jobs include:
Medical Writer (Remote)

Medical Writer (Remote)

TechData Service Company LLC

OR • Remote

$85 - $90/hr

Contractor

Medical, Dental

Posted 14 days ago


Job description

Company: Biotechnology Company

Title: Medical Writer

Contract Position - 6 months with potential extension

Position Summary
Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in support of clinical development and regulatory submissions. This role will partner with Clinical Development, Regulatory Affairs, Biostatistics, Medical Affairs, Quality Assurance, and external vendors to produce clear, accurate, and compliant documents.
Key Responsibilities
Author, review, and edit clinical and regulatory documents, including protocols, protocol amendments, clinical study reports, investigator’s brochures, informed consent forms, CTD clinical modules, briefing documents, safety reports, and responses to regulatory questions.
Support clinical development activities by helping prepare clinical development plans, protocols, and related study documents.
Interpret complex clinical and scientific data and communicate findings clearly and accurately.
Ensure documents comply with ICH, GCP, FDA, EMA, and other applicable regulatory guidelines.
Collaborate with cross-functional teams to manage document timelines, review cycles, and submission-ready deliverables.
Review documents prepared by internal teams or external vendors for clarity, consistency, scientific accuracy, and regulatory compliance.
Qualifications
Advanced degree preferred, such as PhD, PharmD, MD, or MSc in Life Sciences, Medicine, Pharmacy, or a related field.
Minimum 3–5 years of medical writing experience in the pharmaceutical, biotech, or CRO industry.
Strong experience writing clinical trial and regulatory submission documents.
Knowledge of drug development, clinical research, clinical study conduct, regulatory requirements, and biostatistical concepts.
Familiarity with medical terminology and coding dictionaries such as MedDRA and WHODrug.
Strong knowledge of ICH/GCP and regulatory submission requirements.
Epilepsy or neurology experience is a plus.
Veeva experience preferred.
Proficiency with Microsoft Word, Excel, PowerPoint, Adobe Acrobat, EndNote, and document management systems.
Ideal Candidate
The ideal candidate is a detail-oriented medical writer who can manage multiple projects, work independently, collaborate effectively with cross-functional teams, and produce clear, well-structured, submission-ready clinical and regulatory documents.

Company Description

www.techdataservice.com