Chicago, IL · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Author and review Clinical Study Reports (CSRs) and other regulatory documents. * Interpret ...
Quick apply
Chicago, IL · Remote
$50 - $90/hr
Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Author and review Clinical Study Reports (CSRs) and other regulatory documents. * Interpret ...
Chicago, IL · Remote
$50 - $80/hr
Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50-$80/hour ... Author and review Clinical Study Reports (CSRs) and other regulatory documents. * Interpret ...
Quick apply
Chicago, IL · Remote
$50 - $80/hr
Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50-$80/hour ... Author and review Clinical Study Reports (CSRs) and other regulatory documents. * Interpret ...
Chicago, IL · Remote
$50 - $80/hr
Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical ... Required Skills * Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 ...
Quick apply
Chicago, IL · Remote
$50 - $80/hr
Remote Job Type: Contractor Pay: $50-$80/hour Job Overview We are seeking an experienced Medical ... Required Skills * Regulatory Medical Writing * Clinical Study Report (CSR) Authoring * ICH E3 ...
Chicago, IL · On-site +1
Remote and hybrid working options as standard * Continuous learning and professional development ... Job code: CPT407 Career opportunities Medical writing Role Publications Locations USA (Remote ...
Chicago, IL · On-site +1
Remote and hybrid working options as standard * Continuous learning and professional development ... Job code: CPT407 Career opportunities Medical writing Role Publications Locations USA (Remote ...
The S enior Strategic Medical Writer is responsible for leading and writing clinical and regulatory ... Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or ...
New
Quick apply
The S enior Strategic Medical Writer is responsible for leading and writing clinical and regulatory ... Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or ...
New
The S enior Strategic Medical Writer is responsible for leading and writing clinical and regulatory ... Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or ...
The S enior Strategic Medical Writer is responsible for leading and writing clinical and regulatory ... Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or ...
North Chicago, IL · On-site +1
$96K/yr
The S enior Strategic Medical Writer is responsible for leading and writing clinical and regulatory ... Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or ...
North Chicago, IL · On-site +1
$96K/yr
The S enior Strategic Medical Writer is responsible for leading and writing clinical and regulatory ... Prepares clinical and regulatory documents needed for the development of AbbVie drugs and/or ...
Chicago, IL · Remote
$85K - $95K/yr
... writing and medical device regulatory affairs or a Ph.D. with at least 3 years of experience Location & Travel Requirements * This is a remote role (candidates must be based in the United States)
Chicago, IL · Remote
$85K - $95K/yr
... writing and medical device regulatory affairs or a Ph.D. with at least 3 years of experience Location & Travel Requirements * This is a remote role (candidates must be based in the United States)
Chicago, IL · Remote
$155K - $213K/yr
Collaborate with Clinical Operations, Medical Writing, and other internal functions to review and ... Nationwide Remote We are committed to offering competitive compensation. Starting pay is determined ...
Chicago, IL · Remote
$155K - $213K/yr
Collaborate with Clinical Operations, Medical Writing, and other internal functions to review and ... Nationwide Remote We are committed to offering competitive compensation. Starting pay is determined ...
Chicago, IL · Remote
$50 - $80/hr
Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced ... Prepare structured, guideline-based written feedback. Required Qualifications * 5+ years of ...
Quick apply
Chicago, IL · Remote
$50 - $80/hr
Regulatory Affairs Specialist Location: Remote Job Type: Contract We are seeking an experienced ... Prepare structured, guideline-based written feedback. Required Qualifications * 5+ years of ...
Chicago, IL · Remote
$30 - $60/hr
Create and curate source materials such as product specifications, SME notes, regulatory documents ... medical devices, or regulated industries. * Strong ability to create precise, testable technical ...
New
Quick apply
Chicago, IL · Remote
$30 - $60/hr
Create and curate source materials such as product specifications, SME notes, regulatory documents ... medical devices, or regulated industries. * Strong ability to create precise, testable technical ...
New
Chicago, IL · On-site +1
$225K - $260K/yr
Multiple U.S. Offices + Virtual Option (Remote Available) Experience: 4-6 Years Preferred ... Strong legal writing and communication skills * Admission to practice law in the applicable state ...
Quick apply
Chicago, IL · On-site +1
$225K - $260K/yr
Multiple U.S. Offices + Virtual Option (Remote Available) Experience: 4-6 Years Preferred ... Strong legal writing and communication skills * Admission to practice law in the applicable state ...
Chicago, IL · Remote
$110K - $150K/yr
Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians ... Experience with complex medical devices, such as some combination of: * Genomics * NGS * Software ...
Chicago, IL · Remote
$110K - $150K/yr
Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians ... Experience with complex medical devices, such as some combination of: * Genomics * NGS * Software ...
Chicago, IL · On-site +1
$110K - $150K/yr
Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians ... Experience with complex medical devices, such as some combination of: * Genomics * NGS * Software ...
Chicago, IL · On-site +1
$110K - $150K/yr
Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians ... Experience with complex medical devices, such as some combination of: * Genomics * NGS * Software ...
Chicago, IL · Remote
$40 - $48/hr
Remote role in the United States Under general supervision, work with the Senior Manager Regulatory ... written communication and organizational skills Experience with MS Office Suite and Ithos a plus ...
Chicago, IL · Remote
$40 - $48/hr
Remote role in the United States Under general supervision, work with the Senior Manager Regulatory ... written communication and organizational skills Experience with MS Office Suite and Ithos a plus ...
Chicago, IL · Remote
$50 - $70/hr
Document audit results and provide clear written explanations to support AI training and ... Strong understanding of medical coding guidelines, compliance regulations, and audit methodologies.
Quick apply
Chicago, IL · Remote
$50 - $70/hr
Document audit results and provide clear written explanations to support AI training and ... Strong understanding of medical coding guidelines, compliance regulations, and audit methodologies.
Chicago, IL · On-site +1
$190K - $210K/yr
Job Type Remote Job Location This position offers flexibility in work location! For candidates ... Collaborate closely with Sales, Marketing, Finance, Quality & Regulatory, Medical Education ...
Chicago, IL · On-site +1
$190K - $210K/yr
Job Type Remote Job Location This position offers flexibility in work location! For candidates ... Collaborate closely with Sales, Marketing, Finance, Quality & Regulatory, Medical Education ...
Chicago, IL · Remote
$50 - $80/hr
Job Title: Medical Coder Job Type: Contractor Location: Remote Job Overview We are seeking ... Collaborate with project teams through written and verbal communication to improve AI training data ...
Quick apply
Chicago, IL · Remote
$50 - $80/hr
Job Title: Medical Coder Job Type: Contractor Location: Remote Job Overview We are seeking ... Collaborate with project teams through written and verbal communication to improve AI training data ...
Deerfield, IL · On-site +1
Remote/Commuter Opportunity - Open to candidates within the United States SUMMARY: The Senior ... Excellent oral and written communication skills across all levels of the organization, including ...
Deerfield, IL · On-site +1
Remote/Commuter Opportunity - Open to candidates within the United States SUMMARY: The Senior ... Excellent oral and written communication skills across all levels of the organization, including ...
Deerfield, IL · On-site +1
Remote/Commuter Opportunity - Open to candidates within the United States SUMMARY: The Senior ... Excellent oral and written communication skills across all levels of the organization, including ...
Deerfield, IL · On-site +1
Remote/Commuter Opportunity - Open to candidates within the United States SUMMARY: The Senior ... Excellent oral and written communication skills across all levels of the organization, including ...
$13.96 - $17.87
3% of jobs
$17.87 - $21.78
9% of jobs
$25.62 is the 25th percentile. Wages below this are outliers.
$21.78 - $25.70
13% of jobs
$25.70 - $29.61
7% of jobs
$29.61 - $33.52
8% of jobs
$33.52 - $37.44
5% of jobs
The median wage is $39.15 / hr.
$37.44 - $41.35
8% of jobs
$41.35 - $45.26
16% of jobs
$46.78 is the 75th percentile. Wages above this are outliers.
$45.26 - $49.18
12% of jobs
$49.18 - $53.09
7% of jobs
$53.09 - $57.01
11% of jobs
$13
$38
$57
| Aspect | Remote Regulatory Medical Writer | Remote Medical Writer |
|---|---|---|
| Credentials | Medical degree, regulatory writing experience, certifications (e.g., RAC) | Medical, scientific, or related degree; writing experience |
| Work Environment | Pharmaceutical/biotech companies, CROs, regulatory agencies | Pharmaceutical, biotech, healthcare, or scientific organizations |
| Industry Usage | Regulatory submissions, INDs, NDAs, safety reports | Research publications, clinical trial documentation, scientific publications |
| Search/Comparison Intent | Regulatory documentation, compliance, submission writing | Scientific writing, research, publication |
The main difference is that Remote Regulatory Medical Writers focus on preparing regulatory documents for drug approvals and compliance, often requiring specific regulatory knowledge and certifications. Remote Medical Writers have a broader scope, including scientific publications and research documentation. Both roles require strong writing skills and relevant scientific backgrounds, but Regulatory Medical Writers specialize in regulatory submissions and compliance processes.
The top searched job categories for Remote Regulatory Medical Writer jobs in Park Ridge, IL are:
Cities near Park Ridge, IL with the most Remote Regulatory Medical Writer job openings:
$50 - $90/hr
Full-time
Posted 14 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.
