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!
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
- 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
Requirements
- At least 3 years of experience in Sponsor funded Clinical Trials
- Ability to work independently
- Direct patient care experience
- Regulatory knowledge
