Role OverviewThe Clinical Research Coordinator 2 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 strong communication skills, be able to work collaboratively with others, and have the ability to learn new procedures, technologies, and protocols.
Requirements
- Bachelor's degree in a relevant field
- Minimum 2 years of relevant experience
- Learning Agility
- Teamwork
- Technical Proficiency
- Communication
Benefits
- Competitive salary
- Comprehensive benefits package
- Medical, dental, tuition remission
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