**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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