In this role, you will be responsible for implementation of clinical research protocols under physician investigator guidance and delegation and clinical research specialist and/or clinical research coordinator II guidance.
In this role, you will assists the clinical research team in overall study coordination, including, but not limited to, preparing for study initiation and activation, acquisition of source documents, record maintenance, preparing study documents, patient registration, coordinating and data entry.
In this role, you will conduct patient interviews, explains policies and procedures to patient/significant others, reviews the patient's chart and answers questions correctly and courteously. The selected candidate will be adhering to protocol; performs the administration of the agent, electrocardiograms, IV placement, phlebotomy, specimen collection, vitals, patient and adverse event assessment.
Coordinates various aspects of research study, including preparation or necessary documents, patient recruitment, enrollment and follow-up. Organization of study visits, scheduling and communication with investigational pharmacy and laboratories.