Clinical Research Coordinator

Urology Associates Of Central California is currently looking for a Clinical Research Coordinator to join our team. The ideal candidate must be a self starter and be able to manage multiple projects, previous experience as a Research Coordinator and is familiar with the medical field. Two years of experience needed as a Clinical Research specifically in patient facing roles with clinical trials. Knowledge of clinical trial protocols, regulatory guidelines. Medical background or certification in clinical research is strongly preferred.

The Clinical Research Coordinator performs a variety of clinical study activities to assist the Principal Investigator in the conduct of a clinical study.

• Coordinate protocol related research procedures, study visits and follow up care.
• screen recruit and enroll patients research participants
• ensure adherence to IRB approved protocols and regulatory guidelines ( FDA,GCP)
• participate in in the informed consent process for study subjects
• maintain study source documentation and ensure data integrity
• monitor the safety of clinical research patients research participants
• report and document adverse events accurately and promptly
• assist in managing study timelines and meeting protocols milestones

Minimum 2 years of experience as a Clinical Research Coordinator specifically in patient facing roles with clinical trials.

Knowledge of clinical trial protocols, regulatory guidelines and IRB submissions

Experience managing clinical study timelines, patient consent processes, and protocol compliance

Medical background or certification in clinical research (SOCRA or ACRP) is strongly preferred

Proficiency in Microsoft Office and experience with electronic health systems or willingness to learn.

Phlebotomy experience preferred nut not required.