Clinical Research Coordinator: Impact & Compliance

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

Job summary

The Providence Medical Foundation seeks a Clinical Research Coordinator to oversee day-to-day functions of multiple clinical studies under the supervision of the Medical Office Administrator. You will interface with the Principal Investigator, Sponsor, and IRB to ensure timely, accurate documentation and strict GCP/ICH compliance.

This role supports patient-focused care, collaboration with a cross-functional team, and professional growth within Providence's network.

Qualifications

• Completion of an accredited Medical or Phlebotomy training program or equivalent educ/experience
• 2 years experience in a Clinical Research setting, 3 years preferred
• Phlebotomy Certificate upon hire for department SJuHMG Clinical Trials

Responsibilities

• Oversee day-to-day functions of multiple clinical research studies.
• Interface with the Principal Investigator, Sponsor, and the IRB.
• Ensure documentation is timely and accurate; enforce strict GCP/ICH protocol compliance.

Education

Accredited Medical or Phlebotomy training program or equivalent education/experience

Phlebotomy Certificate upon hire

College degree (Bio / Science)

Job description

The Providence Medical Foundation seeks a Clinical Research Coordinator to oversee day-to-day functions of multiple clinical studies under the supervision of the Medical Office Administrator. You will interface with the Principal Investigator, Sponsor, and IRB to ensure timely, accurate documentation and strict GCP/ICH compliance.

This role supports patient-focused care, collaboration with a cross-functional team, and professional growth within Providence's network.