**Seeking a Clinical Research Coordinator in Greenville, NC**
Job Title: Research Coordinator
Position Type : Full-Time
Reports To: Clinical Trials Supervisor
Pay: $60,000-75,000 (Depending on experience)
Position Summary
The research coordinator is primarily responsible for coordinating research patient visits according to both the International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines and the Institutional Review Board (IRB)-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.
Duties:
Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
Administer sponsor required questionnaires (i.e. Visual Function Questionnaire [VFQ])
Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand
Ensures study staff is properly trained on study-related information (i.e. protocol, Informed
Consent Form [ICF], manuals, etc.) and that the training is documented
Creates, manages, and maintains source documents for each trial
Attends teleconferences and Investigator Meetings as requested by research director
Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections
Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals
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