- The CRC thoroughly understands all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator.
- Communicates closely with the sponsor's Clinical Research Associate (CRA) to facilitate the sponsor monitoring and data maintenance process.
- The Clinical Research Coordinator completes all monitor and sponsor queries in a timely manner.
- Track enrollment status of patients and ensure timely communication with patients regarding their study participation.
- Assess eligibility of potential patients and oversee patient enrollment to ensure that informed consent is properly obtained and documented.
- Coordinates and conducts patient visits (drawing blood, collecting vital signs, performing ECGs, and processing specimens).
- Keeps all source documentation up-to-date
- Bachelor's degree Preferred
- 2 year of Clinical Research experience required
- Ophthalmology experience preferred
- Phlebotomy skills are a plus
- Ability to work well both independently and as part of a team
- Ability to handle multiple tasks simultaneously
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Clinical Research Coordinator 226897 - Fort Lauderdale, United States - Medix™
Description
Do you love Clinical Research and want your next career step to be someplace with a lot of upward mobility and growth potential? We are looking for a Clinical Research Coordinator to join our growing team Competitive salary, and a comprehensive benefits package are offered including, medical, dental, vision and 401k.
Overview
The Clinical Research Coordinator (CRC) is responsible for overseeing the day-to-day operations of clinical research trials designed to test the safety and effectiveness of new drugs. The CRC plans and directs clinical research studies – working directly with patients to guide them successfully through the clinical trial process.
Duties
Education
Experience.
Additional Skills for the Clinical Research Coordinator