- Monitor patient eligibility, safety, and data and initiate appropriate action as appropriate
- Ensure detail-oriented contributions are of high-quality and in compliance with regulatory requirements
- Provide input in all stages of the clinical trial, from start-up to close-out
- Scientifically support Clinical Development Phase 1, 2, 3; Data cleansing and analysis.
- BA/BS
- Advanced Clinical/Science Degree preferred (ei; PharmD, PhD, MSN, MPH)
- 2-5 years experience as Clinical Scientist
- At least 4 years of Clinical Trial experience; Phase 1, 2, 3
- Extensive experience with data analysis and review
- Strong computer skills; Microsoft Office Suite (Word, PowerPoint and Excel), EDC RAVE, Spotfire
- Occasional travel.
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