GENERAL SUMMARY OF DUTIES: The Clinical Research Coordinator is responsible for the daily management of the clinical trial activities. The CRC must be self-directed, able to function independently, and have an in-depth understanding of the study protocol(s). The CRC is responsible for coordinating and conducting all aspects of the clinical study and the communication with the Principal Investigator(s).
Knowledge, Skills & Abilities: Previous research experience, lab specimen collecting and processing, phlebotomy, ECG testing, organization of files, patient calendar visits, attention to detail, high energy with determination to achieve desired results of the company and clinical study sponsor. Excellent communication skills; oral and written. Honest, self-starter requires little direction to achieve desired results.