Role OverviewThe Clinical Trial Coordinator will serve as the coordinator for a variety of clinical trials and/or studies, providing active leadership and control of all assigned clinical trials and studies in which the department is participating. The incumbent will perform all usual and necessary diagnostic testing required by those clinical trials to the ability of their level of skills and/or certification. The position requires recruiting patients for assigned studies, working with administrators and physicians, and maintaining accurate records.
What You Will Do
The main day-to-day responsibilities of the Clinical Trial Coordinator include classifying and maintaining all study records, familiarizing with study protocols, collecting and coding data, ensuring compliance with protocol guidelines, interacting with scheduling personnel, and maintaining accurate records of patient visits and compliance.
Why It Might Be a Fit
The ideal candidate will have a strong attention to detail, the ability to manage multiple assignments simultaneously, and excellent organizational skills. The position demands adaptability and flexibility in responding to changing priorities and schedules, while maintaining a high level of professionalism.
Requirements
- Bachelor's degree
- Three years research experience
- Certification as a Certified Research Assistant/Coordinator
- Certification at the Certified Ophthalmic Assistant level (COA)
- Successful completion of a formal, one year CAAHEP approved training course
Benefits
- Competitive salary
- Benefits package
- Opportunities for professional growth and development
- Flexible work environment
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