San Jose, CA · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Quick apply
San Jose, CA · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Boston, MA · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Quick apply
Boston, MA · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Miami, FL · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Quick apply
Miami, FL · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
San Francisco, CA · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Quick apply
San Francisco, CA · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
San Jose, CA · On-site
$50 - $80/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
San Jose, CA · On-site
$50 - $80/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Groton, CT · On-site
Groton, CT Duration: 3 years+ Our client is looking to hire the Medical Writer Company is looking ... Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic ...
Groton, CT · On-site
Groton, CT Duration: 3 years+ Our client is looking to hire the Medical Writer Company is looking ... Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic ...
Washington, DC · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Quick apply
Washington, DC · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Review safety documentation, including DSURs and PSURs/PBRERs. * Provide structured feedback and ...
Sandy, UT · On-site
Medical Affairs is responsible for ensuring the safety and efficacy of Medication Delivery Solutions (MDS) products worldwide. * The Medical Writer will support this mission by assisting with and ...
Sandy, UT · On-site
Medical Affairs is responsible for ensuring the safety and efficacy of Medication Delivery Solutions (MDS) products worldwide. * The Medical Writer will support this mission by assisting with and ...
Durham, NC · On-site
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety ... Mentor and support other medical writers, ensuring high-quality, scientifically sound, and ...
Durham, NC · On-site
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety ... Mentor and support other medical writers, ensuring high-quality, scientifically sound, and ...
Durham, NC · On-site
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety ... Mentor and support other medical writers, ensuring high-quality, scientifically sound, and ...
Durham, NC · On-site
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety ... Mentor and support other medical writers, ensuring high-quality, scientifically sound, and ...
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety ... Mentor and support other medical writers, ensuring high-quality, scientifically sound, and ...
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety ... Mentor and support other medical writers, ensuring high-quality, scientifically sound, and ...
Durham, NC · On-site
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety ... Mentor and support other medical writers, ensuring high-quality, scientifically sound, and ...
Durham, NC · On-site
Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety ... Mentor and support other medical writers, ensuring high-quality, scientifically sound, and ...
Blue Bell, PA · On-site
Senior Medical Writer- ICON- Remote USA ICON is a global healthcare intelligence and clinical ... safety summaries, biostatistical tables, published articles, etc), and its accurate, concise ...
Blue Bell, PA · On-site
Senior Medical Writer- ICON- Remote USA ICON is a global healthcare intelligence and clinical ... safety summaries, biostatistical tables, published articles, etc), and its accurate, concise ...
Madison, NJ · On-site
Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and biotherapeutic ... An advanced degree preferred and at least 3 years medical writing experience and /or experience in ...
Madison, NJ · On-site
Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and biotherapeutic ... An advanced degree preferred and at least 3 years medical writing experience and /or experience in ...
Pennington, NJ · On-site
Medical Writer Location: Pennington, New Jersey-08534 Duration: 6 Months Scientific Writer for ... documents, aggregate safety reports, risk management plans), ensuring the coordination and ...
Pennington, NJ · On-site
Medical Writer Location: Pennington, New Jersey-08534 Duration: 6 Months Scientific Writer for ... documents, aggregate safety reports, risk management plans), ensuring the coordination and ...
Collegeville, PA · On-site
The Medical Writer is responsible for medical documentation summarizing risks and benefits in ... Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic ...
Collegeville, PA · On-site
The Medical Writer is responsible for medical documentation summarizing risks and benefits in ... Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic ...
The Senior Medical Writer applies advanced documentation preparation and document project ... Drafts and edits documents used in reporting aggregate safety and efficacy information for a ...
The Senior Medical Writer applies advanced documentation preparation and document project ... Drafts and edits documents used in reporting aggregate safety and efficacy information for a ...
$172K - $232K/yr
... and safety summaries, and related documents. Other documents may include informed consent forms ... Provide medical writing subject matter expertise and leadership to project teams and collaborate ...
$172K - $232K/yr
... and safety summaries, and related documents. Other documents may include informed consent forms ... Provide medical writing subject matter expertise and leadership to project teams and collaborate ...
The Senior Medical Writer applies advanced documentation preparation and document project ... Drafts and edits documents used in reporting aggregate safety and efficacy information for a ...
The Senior Medical Writer applies advanced documentation preparation and document project ... Drafts and edits documents used in reporting aggregate safety and efficacy information for a ...
Peapack, NJ · On-site
... and safety questions from regulatory authorities. Provide project teams with expertise on ... Support clinical teams by providing analyses of clinical data, reviews of the medical literature ...
Peapack, NJ · On-site
... and safety questions from regulatory authorities. Provide project teams with expertise on ... Support clinical teams by providing analyses of clinical data, reviews of the medical literature ...
$11.54 - $17.66
0% of jobs
$17.66 - $23.78
8% of jobs
$23.78 - $29.90
12% of jobs
$32.80 is the 25th percentile. Wages below this are outliers.
$29.90 - $36.01
11% of jobs
$36.01 - $42.13
11% of jobs
The median wage is $44.87 / hr.
$42.13 - $48.25
20% of jobs
$54.04 is the 75th percentile. Wages above this are outliers.
$48.25 - $54.37
15% of jobs
$54.37 - $60.49
13% of jobs
$60.49 - $66.61
7% of jobs
$66.61 - $72.73
2% of jobs
$72.73 - $78.85
2% of jobs
$11
$46
$78
Cities with the most Safety Medical Writer job openings:
States with the most job openings for Safety Medical Writer jobs include:
For Safety Medical Writer jobs, the most frequently searched job titles are:
San Jose, CA • Remote
$50 - $90/hr
Full-time
Re-posted 3 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.
