Senior Clinical Research Coordinator - Pediatrics Hematology & Oncology

Senior Clinical Research Coordinator – Pediatrics Hematology & Oncology

Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
Basic Life Support certification must be obtained within one month of hire date.
Clinical Research (3 Years)
Supervision

Manages protocol study start up and study launch, submission, and maintenance of essential regulatory documents.
Assists in budget review and invoice tracking.
Assists in scheduling and facilitating site visits by external and internal monitors and auditors.
Works with PI to evaluate research procedures; confers with PI to assist in developing plans for research projects; provides input of feasibility, cost, and workload in regards to participating in new clinical trials.
Serves as a resource to clinical research staff, ensuring appropriate procedures and research projects are completed according to IRB and federal guidelines.
May participate in the hiring, training, and evaluation of clinical research staff.
Serves as a subject matter expert for clinical group and acts as a resource for protocol related questions.
Facilitates communication with PIs to ensure that study objectives are met in a timely manner; maintains a cooperative relationship with Hematology/Oncology and other divisions and departments.
Provides study coordinator functions and performs all duties associated with the coordination and implementation of clinical research study/projects, data collection, and the management of data generated by study protocols; consents participants for non-therapeutic clinical trials.
Performs other duties incidental to the work described above.