Clinical Research Coordinator: Study Operations & Compliance

Providence; Fullerton (CA); Hybrid; USD 46,000 - 71,000; Full time

Job summary

Providence Clinical Network in Fullerton, CA seeks a Clinical Research Coordinator to oversee day-to-day study operations, interfacing with the PI, patients, and sponsor while ensuring timely, accurate documentation and strict adherence to GCP/ICH protocols. The role partners with investigators to support multiple trials and ensure regulatory compliance.

The position emphasizes hands-on study coordination, documentation quality, and collaboration within a team focused on patient-centered

Qualifications

• Coursework/Training completing an accredited Medical or Phlebotomy program or 2 years clinical research experience.
• HS Diploma or GED or equivalent educ/experience.
• 2 years experience in a Clinical Research setting.
• Graduate of a Vocational School or college is preferred.
• Phlebotomy Certificate may be required upon hire for certain departments.

Responsibilities

• Oversees day-to-day functions of multiple clinical research studies.
• Interfaces with Principal Investigator, patients, Sponsor, and IRB.
• Ensures documentation is timely and accurate and complies with study protocols (GCP/ICH).

Skills

Clinical Research Experience

Phlebotomy Training

Education

HS Diploma or GED

Vocational School/College

Job description

Providence Clinical Network in Fullerton, CA seeks a Clinical Research Coordinator to oversee day-to-day study operations, interfacing with the PI, patients, and sponsor while ensuring timely, accurate documentation and strict adherence to GCP/ICH protocols. The role partners with investigators to support multiple trials and ensure regulatory compliance.

The position emphasizes hands-on study coordination, documentation quality, and collaboration within a team focused on patient-centered