What are the responsibilities and job description for the Clinical Research Coordinator I position at arizona?
- Screen, recruit, and enroll participants for medical studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met.
- Evaluate potential study participants to ensure they meet eligibility requirements, instruct study participants concerning research protocol, and complete the patient informed consent procedure.
- Schedule and/or perform medical testing per protocol such as drawing blood, vital signs, EKGs, etc., includes processing and packaging of laboratory samples for shipment.
- Assess participants during clinic visit; perform initial review of study lab results; determine if patient is experiencing side effects or other problems; and notify principal investigator if problems arise.
- Complete case report forms for each study participant and document medical data in the patient record and sponsor database. Ensure case report forms or other data collection/tracking tools are created if not provided by sponsor.
- Participate in sponsors site visits for assigned studies.
- Occasional out-of-state travel may be required for sponsor training.