Are you looking for a new job within Clinical research? We are looking for a Clinical Research Coordinator (CRC) who loves research to join our growing team. This role does require prior Clinical Research experience in some capacity.

Phlebotomy experience required!

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical
trials under the direction of the Director/Manager of Clinical Site Operations and the Principal Investigator
or designee. Working in collaboration with the Principal Investigator, the CRC is a critical member of our
organization and contribute to patient enrollment efforts in a variety of clinical trials. And will implement
and coordinate research study procedures for the successful management of clinical trials.

* Manages clinical research studies and adheres to Standard Operating Procedures (SOPs),
Good Clinical Practices (GCPs), study protocols, clinical trial agreements, and regulations governing
clinical research. Regularly interfaces with current and potential clinical trial participants to determine
eligibility and consent of study participants in alignment with the clinical trial protocol
* Coordinate research participant visits and study-related procedures according to study protocol
windows and study team schedules, which many involve handling travel logistics for research
participants; ensure reminder communications (phone, text, or email) are sent to promote research
participant show rate and compliance; identity and outreach to prospective patients; prepare study visit
materials such as lab kits, study form, and diaries for participants visits

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