- Listed at $100 an hour
- 5 to 20 hours a week
- Remote
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This Role at a Glance
- Who it is for: It suits professionals with at least five years in clinical research, biomedical science, or regulatory affairs, plus hands-on experience authoring or reviewing these materials.
- Pay: Listed at $100 an hour on 2026-11-13.
How to Apply in 3 Steps
- Check that you meet the requirements and live where the role is open.
- Select Apply now on this page. The application opens in a new tab.
- Expect an interview. AI tools write its follow-up questions and help evaluate it.
You will write, review, and improve AI-generated documents, spreadsheets, and slide decks for clinical development, such as study reports, protocol synopses, and regulatory submissions. The role is fully remote, with flexible hours of 5 to 20 per week.
- Field: Medical
- Posted 2026-08-15
Pay as listed on 2026-11-13.
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Questions About This Role
What Experience Does the Clinical and Biomedical Specialist Role Expect?
Applicants should have hands-on history writing or reviewing clinical study reports, protocol synopses, or regulatory dossier modules at a pharma, biotech, or CRO. The tasks also call for roughly five or more years in clinical research, biomedical science, or regulatory affairs.
Which Regulatory Standards Matter for the Pharma Consultant AI Training Role?
The requirements stress deep familiarity with ICH-GCP, plus FDA and EMA expectations. You would need to apply that rigor to materials like investigator brochures and medical affairs content while judging AI-generated work.
Before You Apply
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