Clinical Research Coordinator
St. Joseph's Candler
- Savannah, GA
- Permanent
- Full-time
- Monitor study activities for assigned protocols to ensure compliance with study requirements as well as local, federal, state, and institutional regulatory policies. Maintains all documents and records related to study activities including case report forms, source documents, pharmacy drug binders, and regulatory documents.
- Assess eligibility of potential subjects using a variety of methods such as the review of medical records and discussions with physicians and Advanced Practice Providers. Be actively involved in patient recruitment by discussing potential subjects with investigators, approaching candidates in the office or speaking to them by phone, asking pre-screening eligibility questions, reviewing the trial with the patient, and conducting informed consent with the patient.
- Schedule and oversee participant visits and any required tests and/or imagining according to the protocol. Ensure visits, tests, and imaging appointments are scheduled within the appropriate window and completed at each required timepoint. Monitor and facilitate patient compliance with medication and ensure drug accountability is maintained for assigned protocols.
- Monitor subjects per protocol requirements and ensure that the modification of study treatment is overseen by the investigator and/or CRC under the supervision of the investigator. Monitor patients throughout the trial for all untoward reactions and communicate immediately to the investigator.
- Document and report adverse events, ensuring review and follow-up by the treating physician. Monitor patient care and treatment side-effects together with the investigator while keeping detailed documentation for reporting and source documentation.