Description: Clinical Research Coordinator - Lakeland, FL (33812)

The Clinical Research Coordinator conducts clinical research visits in accordance with ICH-
GCP, Clinical Research SOPs and sponsor protocols.

Essential Duties and Responsibilities:
● Understand clinical trial protocols (rationale, inclusion/exclusion criteria, study design,
study medication and comparators, mechanism of action, required procedures, etc).
● Review detailed medical records including electronic medical records, lab reports,
biopsies, radiology scans and other related medical data to confirm if a patient is
eligible for a clinical trial.
● Liaise with other clinical research staff, medical providers and clinic staff to coordinate
screening activities including but not limited to confirming patient eligibility,
scheduling consents, placing screening orders to support patient randomization.
● Communicate individual patient and study level details with clinical trials sponsors,
contract research organizations and other external providers.
● Document patient and study level activities in clinical trial management systems,
tracking documentation and electronic medical records.
● Support management of regulatory documentation, investigational product storage
and accountability as well as clinical data entry and query resolution
● Perform clinical trial visits with patients in partnership with clinic staff and providers in
accordance with clinical trial protocols.
● Performs additional tasks as assigned by clinical research or clinic leadership.
● Responsible for overall conduct of assigned clinical research responsibilities.

Education:
● Bachelor's degree or equivalent combination of other degrees or certifications
(nursing, phlebotomy, medical assistant, etc) and experience

Skills:
● 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

Pay: $28 - 35/hr