Clinical Research Coordinator: Drive Study Success

Providence; Fullerton (CA); On-site; USD 45,000 - 70,000; Full time

Job summary

Providence Clinical Network is seeking a Clinical Research Coordinator to oversee day-to-day activities across multiple studies in a patient-centered environment. You will collaborate with the PI, patients, sponsors, and the IRB to ensure timely, accurate documentation and strict adherence to study protocols.

The role emphasizes GCP/ICH compliance, data integrity, and close coordination with the research team.

Qualifications

• Completion of an accredited Medical or Phlebotomy training program, or 2 years of clinical research experience.
• High school diploma or GED, or equivalent education/experience.
• 2 years experience in a clinical research setting.
• Preferred: 3 years experience in a clinical research setting.
• Graduate of a vocational school (preferred).

Responsibilities

• Oversee day-to-day functions of multiple clinical research studies.
• Interface with the Principal Investigator, patient, Sponsor, and the IRB.
• Ensure documentation is timely and accurate and maintain strict compliance to study protocols (GCP/ICH).

Skills

GCP/ICH knowledge

Education

Accredited Medical or Phlebotomy training program

High School Diploma or GED

2 years Clinical Research experience

3 years Clinical Research experience

Vocational school graduate

Job description

Providence Clinical Network is seeking a Clinical Research Coordinator to oversee day-to-day activities across multiple studies in a patient-centered environment. You will collaborate with the PI, patients, sponsors, and the IRB to ensure timely, accurate documentation and strict adherence to study protocols.

The role emphasizes GCP/ICH compliance, data integrity, and close coordination with the research team.