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Remote Case Study Writer Jobs in Pennsylvania (NOW HIRING)

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 ...

Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ... by-case basis. Advanced knowledge of ICH and related regulatory guidelines. Excellent written ...

Expert Regulatory Writer

Distant, PA · On-site +1

$151K - $226K/yr

If associate is remote, all home office expenses and any travel/lodging to specific NJ site for ... Study Reports (CSR), Risk Management Plans (RMP),complex CTD submission documents (clinical ...

Global Study Lead

Philadelphia, PA · On-site +1

$144K - $195K/yr

However, for exceptional candidates, remote working arrangements may also be considered. Summary of ... Strong project planning/ management, communication (written and verbal) and presentation skills

Global Study Lead

Philadelphia, PA · On-site +1

$144K - $195K/yr

However, for exceptional candidates, remote working arrangements may also be considered. Summary of ... Strong project planning/ management, communication (written and verbal) and presentation skills ...

Legal Writing & Editing * Court Filings & Case Material Review * Legal Research & Summarization ... Remote Collaboration * Digital Platform Adaptability * Knowledge of Current Statutes & Case Law

Senior Medical Writer- ICON- Remote USA ICON is a global healthcare intelligence and clinical ... study reports, safety summaries, biostatistical tables, published articles, etc), and its accurate ...

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Remote Case Study Writer information

What is the difference between Remote Case Study Writer vs Remote Content Writer?

AspectRemote Case Study WriterRemote Content Writer
CredentialsWriting experience, industry knowledge, sometimes marketing or business backgroundGeneral writing skills, SEO knowledge, content marketing experience
Work EnvironmentFreelance or remote, often project-based, working with businesses or agenciesRemote, creating various content types like blogs, articles, social media posts
Industry UsageCommon in consulting, B2B, tech, healthcare sectorsUsed across multiple industries including marketing, media, education

The main difference is that Remote Case Study Writers focus on creating detailed, industry-specific case studies that showcase client success stories, requiring specialized knowledge. Remote Content Writers produce a broader range of content types for various purposes. Both roles are remote and require strong writing skills, but their focus and output differ significantly.

What cities in Pennsylvania are hiring for Remote Case Study Writer jobs?

Cities in Pennsylvania with the most Remote Case Study Writer job openings:

Medical Writer - Remote

YO AI Labs

Philadelphia, PA • Remote

$50 - $90/hr

Full-time

Posted 21 days ago


Job description

Job Title: Medical Writer Expert Remote

Location: Remote
Job Type: Contractor
Pay: $50–$80/hour

Job Overview

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 Responsibilities
  • Author 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.

Required Skills
  • 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

Qualifications
  • 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.