- Understand clinical trial protocols (rationale, inclusion/exclusion criteria, study design,
- Review detailed medical records including electronic medical records, lab reports,
- Liaise with other clinical research staff, medical providers and clinic staff to coordinate
- Communicate individual patient and study level details with clinical trials sponsors,
- Document patient and study level activities in clinical trial management systems,
- Support management of regulatory documentation, investigational product storage
- Perform clinical trial visits with patients in partnership with clinic staff and providers in
- Performs additional tasks as assigned by clinical research or clinic leadership.
- Responsible for overall conduct of assigned clinical research responsibilities.
- Bachelor's degree or equivalent combination of other degrees or certifications
- Proficient in Microsoft Office, Outlook, and other Computer Use
- Ability to organize a high-volume workload and prioritize tasks accordingly
- Strong work ethic and personal integrity
- Timeliness and dependability
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clinical research coordinator - Mulberry, FL, United States - Medix
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Description
:Clinical Research Coordinator - Lakeland, FL
The Clinical Research Coordinator conducts clinical research visits in accordance with ICH-GCP, Clinical Research SOPs and sponsor protocols.
Essential Duties and Responsibilities:
eligible for a clinical trial.
scheduling consents, placing screening orders to support patient randomization.
Education:
Skills:
Pay:
$2- 35/hr