Clinical Research Coordinator

Flexible work arrangements, including virtual/hybrid work locations, are an integral part of the School of Medicine’s Working Forward initiative. As such, this position’s work location is designated as hybrid. Please note that the designated work location is subject to change based on the unit’s business needs.

This position will serve as a Clinical Research Coordinator within the Department of Urology. The Clinical Research Coordinator is responsible for the planning, organization, and conduct of multiple clinical research study protocols, including independently collecting and recording data, project administration, and communication with various stakeholders.

This position will contribute professional duties in planning, organizing, conducting, and evaluating research for many oncology and non-oncology clinical trials within the department. Position will require a comprehensive knowledge of research in trial startup and management and will serve to independently manage numerous trials simultaneously, under the supervision of the Research Project Manager and the Clinical Trials Director.

The range of duties include but is not limited to: working with sponsors in feasibility, budget negotiation, contract submission, and following regulatory flow through process up to site activation and enrollment. Project planning and design, database development and management, data/information collection, preparing reports for use in communication with sponsors, monitors, and Director. Responsible for directing a trial from startup to closeout.