Clinical Research Coordinator - Trials & Compliance Leader

Providence; Mission Viejo (CA); Sur place; USD 46 000 - 71 000; Plein temps

Résumé du poste

Providence Medical Foundation seeks a Clinical Research Coordinator to manage day-to-day activities for multiple studies. You will collaborate with the Principal Investigator, patients, sponsors, and the IRB to ensure timely, accurate documentation and strict GCP/ICH protocol adherence.

This role supports Providence's mission, with a focus on safety, quality, and patient-centered care across our California sites. Comprehensive benefits and professional growth opportunities are available.

Qualifications

• Completion of an accredited Medical or Phlebotomy training program, or equivalent education/experience.
• 2 years clinical research experience; 3 years preferred.
• Phlebotomy certificate upon hire for the SJuHMG Clinical Trials department.

Responsabilités

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

Formation

Medical/Phlebotomy training

Clinical Research experience

Phlebotomy certificate

College degree

Description du poste

Providence Medical Foundation seeks a Clinical Research Coordinator to manage day-to-day activities for multiple studies. You will collaborate with the Principal Investigator, patients, sponsors, and the IRB to ensure timely, accurate documentation and strict GCP/ICH protocol adherence.

This role supports Providence's mission, with a focus on safety, quality, and patient-centered care across our California sites. Comprehensive benefits and professional growth opportunities are available.