Clinical Research Coordinator - GCP/ICH & IRB Liaison

Agence PROvidence; Anaheim (CA); On-site; USD 46,000 - 71,000; Full time

Job summary

Providence in California is seeking a Clinical Research Coordinator to support day-to-day operations of multiple trials under the Medical Office Administrator. You will interface with the Principal Investigator, patients, sponsors, and the IRB to ensure timely, accurate documentation and strict adherence to GCP/ICH study protocols.

This role requires completing an accredited medical or phlebotomy training program, with preferred credentials such as a college degree and phlebotomy certification.

Qualifications

• Completion of an accredited medical or phlebotomy training program (or equivalent education/experience).
• Graduate of a vocational school or college.
• Biohazardous material packaging training (preferred).
• F02 AMG Clinical Trials: college degree required.
• Phlebotomy certificate upon hire (for specific department).
• 2 years in a clinical research setting; 3 years preferred.

Responsibilities

• Oversee day-to-day functions of multiple clinical research studies.
• Interface with the Principal Investigator, patient, sponsor, and the IRB to ensure documentation and protocol compliance.

Education

Accredited medical or phlebotomy training

Job description

Providence in California is seeking a Clinical Research Coordinator to support day-to-day operations of multiple trials under the Medical Office Administrator. You will interface with the Principal Investigator, patients, sponsors, and the IRB to ensure timely, accurate documentation and strict adherence to GCP/ICH study protocols.

This role requires completing an accredited medical or phlebotomy training program, with preferred credentials such as a college degree and phlebotomy certification.