Boston, MA · Remote
$50 - $90/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Boston, MA · Remote
$50 - $90/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Houston, TX · Remote
$50 - $90/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Houston, TX · Remote
$50 - $90/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
San Jose, CA · Remote
$50 - $90/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
San Jose, CA · Remote
$50 - $90/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
San Jose, CA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
San Jose, CA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
New York, NY · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
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New York, NY · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Palo Alto, CA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
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Palo Alto, CA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Houston, TX · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Houston, TX · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Atlanta, GA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Atlanta, GA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Miami, FL · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Miami, FL · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Philadelphia, PA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Philadelphia, PA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Boston, MA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Boston, MA · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Senior Regulatory Medical Writer ... Join our colleagues in bringing our Mission to life - enabling our customers to make the world ...
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Senior Regulatory Medical Writer ... Join our colleagues in bringing our Mission to life - enabling our customers to make the world ...
Blue Bell, PA · On-site +1
Significant experience in medical writing, particularly in regulatory submissions and clinical documentation * Strong understanding of regulatory requirements and industry standards for clinical ...
Blue Bell, PA · On-site +1
Significant experience in medical writing, particularly in regulatory submissions and clinical documentation * Strong understanding of regulatory requirements and industry standards for clinical ...
Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin ... ASSOCIATE DIRECTOR - REGULATORY AND MEDICAL WRITING SUMMARY: The Associate Director, Medical ...
Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin ... ASSOCIATE DIRECTOR - REGULATORY AND MEDICAL WRITING SUMMARY: The Associate Director, Medical ...
Washington, DC · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Washington, DC · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Dallas, TX · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
Quick apply
Dallas, TX · Remote
$50 - $80/hr
Strong Written Communication & Collaboration Qualifications * 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment. * Experience authoring Clinical Study ...
With deep domain expertise in regulatory sciences, clinical research solutions, quality ... Independently authors (writes/edits) high-quality medical writing deliverables (i.e., clinical ...
With deep domain expertise in regulatory sciences, clinical research solutions, quality ... Independently authors (writes/edits) high-quality medical writing deliverables (i.e., clinical ...
These are NOT regulatory medical writer positions. As part of our Medical Writing & Scientific ... Cultivate expertise in assigned therapeutic areas * Edit and appropriately reference content ...
These are NOT regulatory medical writer positions. As part of our Medical Writing & Scientific ... Cultivate expertise in assigned therapeutic areas * Edit and appropriately reference content ...
Princeton, NJ · On-site
$80 - $130/hr
Position Summary The medical writer will be responsible for the management and oversight of ... to regulatory authorities in support of marketing applications and BLAs. * Act as a member of ...
Princeton, NJ · On-site
$80 - $130/hr
Position Summary The medical writer will be responsible for the management and oversight of ... to regulatory authorities in support of marketing applications and BLAs. * Act as a member of ...
Princeton, NJ · On-site
$80K - $130K/yr
... to regulatory authorities in support of marketing applications and BLAs. * Act as a member of ... medical writer in the pharmaceutical industry PhD with at least 1 year experience as a medical ...
Princeton, NJ · On-site
$80K - $130K/yr
... to regulatory authorities in support of marketing applications and BLAs. * Act as a member of ... medical writer in the pharmaceutical industry PhD with at least 1 year experience as a medical ...
$14.18 - $18.16
3% of jobs
$18.16 - $22.14
9% of jobs
$26.03 is the 25th percentile. Wages below this are outliers.
$22.14 - $26.11
13% of jobs
$26.11 - $30.09
7% of jobs
$30.09 - $34.07
8% of jobs
$34.07 - $38.05
5% of jobs
The median wage is $39.79 / hr.
$38.05 - $42.02
8% of jobs
$42.02 - $46
16% of jobs
$47.54 is the 75th percentile. Wages above this are outliers.
$46 - $49.98
12% of jobs
$49.98 - $53.96
7% of jobs
$53.96 - $57.93
11% of jobs
$14
$38
$57
| Aspect | Live In Regulatory Medical Writer | Regulatory Medical Writer |
|---|---|---|
| Credentials | Typically requires a life sciences degree and medical writing certification | Same as Live In role, often with additional regulatory training |
| Work Environment | Usually based at a single location, living on-site or nearby | Office-based or remote, depending on employer |
| Employer & Industry | Pharmaceutical, biotech companies, or CROs | Pharmaceutical, biotech, or regulatory agencies |
| Search & Comparison Intent | Often searched by those seeking on-site or live-in roles | More general, including remote or office roles |
Live In Regulatory Medical Writers focus on on-site, live-in roles within pharmaceutical or biotech companies, requiring specific certifications and a preference for on-location work. Regulatory Medical Writers may work remotely or in-office, with similar qualifications, but without the live-in component. The main difference lies in the work setting and living arrangements.
Cities with the most Live In Regulatory Medical Writer job openings:
The most popular types of Regulatory Medical Writer jobs are:
States with the most job openings for Live In Regulatory Medical Writer jobs include:
$50 - $90/hr
Full-time
Posted 18 days ago
Location: Remote
Job Type: Contractor
Pay: $50–$80/hour
We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing.
Key ResponsibilitiesAuthor and review Clinical Study Reports (CSRs) and other regulatory documents.
Interpret clinical protocols and ensure compliance with ICH guidelines.
Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Review safety documentation, including DSURs and PSURs/PBRERs.
Provide structured feedback and collaborate with cross-functional teams.
Support AI-assisted documentation evaluation and quality improvement initiatives.
Regulatory Medical Writing
Clinical Study Report (CSR) Authoring
ICH E3 Guidelines
Scientific Accuracy Assessment
Source Data Verification
Clinical Protocol Interpretation
TFL Analysis
eCTD Knowledge
Strong Written Communication & Collaboration
5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.
Experience authoring Clinical Study Reports and regulatory documentation.
Strong knowledge of ICH E3, ICH E2F, ICH E2C, and eCTD requirements.
Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field (MD, PharmD, PhD, or MSc).
Experience in oncology and haematology is preferred.
