Role OverviewResponsible for coordinating and facilitating daily activities in clinical studies, ensuring compliance with protocols, SOPs, and regulations. Works in a team to set up and conduct studies, prepares and maintains study documentation, and trains new staff. Provides excellent customer service and adheres to safety and operational integrity procedures.
What You Will Do
Coordinates scheduling, prepares study documentation, conducts pre-study meetings, reviews and provides feedback on draft protocols, and orders subject compensation. Assists in IRB and regulatory document submission/review, and leads training workshops. Provides excellent customer service and maintains a positive interaction with peers and supervisors.
Why It Might Be a Fit
The ideal candidate has a bachelor's degree in science or equivalent, 2+ years of relevant work experience, and CCRC/CCRA certification. Must understand basic concepts in clinical research and be capable of learning and performing duties during clinical studies.
Requirements
- Bachelor's degree in science or equivalent
- 2+ years of relevant work experience
- CCRC/CCRA certification a strong plus
- Understanding of basic concepts in clinical research
Benefits
- Excellent customer service
- Positive and respectful interaction with peers and supervisors
- Adherence to safety and operational integrity procedures
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