**Seeking a Clinical Research Coordinator for a Clinical Research site in Sarasota, FL**
The research coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures.
Location: Sarasota, FL
Schedule: Full time; On-Site
Monday-Friday 40 hrs a week
Compensation: $60,000-$75,000
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. 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, 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.
• Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately.
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