Clinical Research Scientist
Job Summary
Supporting clinical trial initiatives, the full-time Clinical Research Scientist will develop study protocols, address scientific inquiries, and assist with regulatory documentation in a remote capacity.
Key responsibilities
- Develop clinical study concept sheets and protocols based on trial design principles
- Prepare study-related documents, including protocols, amendments, and Investigator meeting materials
- Evaluate scientific literature to support new study development and therapeutic-area expansion
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 regulatory reporting
- Ability to review clinical data listings and summary tables
Complete Job Description
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