Role OverviewThe Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines.
What You Will Do
Assists in participant recruitment and retention activities, performs study procedures, collects and processes specimens, maintains study binders and filings, and monitors and reports study unanticipated/adverse events and protocol deviations.
Why It Might Be a Fit
The ideal candidate will have a Bachelor's degree in a relevant field, 2 years of relevant experience, and skills in completing assignments accurately, analyzing and organizing work, and processing confidential information with discretion.
Requirements
- Bachelor's degree in a relevant field
- Minimum 2 years of relevant experience
- Skill in completing assignments accurately and with attention to detail
- Ability to analyze, organize and prioritize work under pressure while meeting deadlines
- Ability to process and handle confidential information with discretion
Benefits
- Competitive salaries
- Comprehensive benefits package
- Medical
- Dental
- Tuition remission
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