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data management training dashboards informed consent irb📋 Description
- Study startup and regulatory coordination
- IRB submission support (Advarra docs)
- Literature reviews for protocol development
- Draft informed consent forms and recruitment materials
- Organize investigator, site, and study files
- Build and QA study questionnaires and data collection tools
🎯 Requirements
- Experience coordinating clinical research
- IRB processes and documentation familiarity
- Strong writing for study materials and reports
- Comfortable with data collection tools and spreadsheets
- Detail-oriented with multiple workstreams
- Interest in peptides and personalized medicine
🎁 Benefits
- Remote, fully-remote role
- Ownership and impact at an early-stage company
- Build a clinical research engine for longevity
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