This position will be primarily based at our St. Vincent's East Location; However, training will occur at St. Vincent's Downtown Birmingham


Description of Duties:

• Screens all potential patients for protocol eligibility. Maintains and submits monthly screening logs.

• Presents trial concepts and details to patients and participate in the informed consent process under the direction of the physicians.

• Ensures potential participants fully understand the study during the informed consent process and documents all consent and/or reconsent appropriately.

• Coordinates study patient's scheduling for tests and treatments required by the protocol.

• Documents any changes in the patient's condition, adverse events, concomitant medication use, protocol compliance, and response to the study drug. Reports all findings and any abnormal results or deviations to an R.N. or physician.

• Accurately reports serious adverse events and pro...