Clinical Research Scientist
Job Summary
Supporting clinical trial design remotely, the full-time Clinical Research Scientist will develop study protocols, contribute to regulatory documentation, and address scientific inquiries while collaborating with clinical investigators.
Key responsibilities
- Develop clinical study concept sheets and protocols based on trial design principles
- Prepare study protocols, amendments, and related clinical documents
- Assist with regulatory documentation and support the review of data listings and study results
Required qualifications
- PharmD with 2+ years, MS with 6+ years, or BS/RN with 8+ years of relevant scientific and/or drug development experience
- Experience in clinical trial design and study development
- Proficiency in clinical study protocol development and amendments
- Knowledge of IND documentation and New Drug Application processes
- Ability to evaluate scientific literature and synthesize findings for study development
Complete Job Description
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