Clinical Research Coordinator
Seeking a Research Coordinator with at least 3 years experience with clinical trials. The candidate will coordinate with the principal investigator, patients, pharmaceuticals, labs and monitors in handling and conducting the full cycle of clinical research trials. This includes document submission to IRB, managing audits and able to handle multiple studies. The candidate must be bilingual (English/Spanish) with excellent skills in writing, communication and quick to understand training and protocols for each study.
The Clinical Research Coordinator (CRC) is responsible for overseeing the day-to-day operations of clinical trials designed to test the safety and effectiveness of new drugs. The CRC plans and directs clinical research studies - working directly with patients to guide them successfully through the clinical trial process - and is responsible for managing clinical trial performance. Team Member in this role are expected to follow Good Clinical Practice (GCP) in the conduct of clinical investigations and to collect, record, and maintain source and sponsor documentation. The candidate should be bilingual (English/Spanish) with good writing skills.
- Bachelor's degree preferred in healthcare related field but not required.
- Certified Clinical Research Coordinator (CCRC) certification preferred.
- Medical Assistant (MA). Licensed Practical Nurse (LPN), Registered Nurse (RN), or other medical licensure or certificate is a plus.