Clinical Research Coordinator

Providence • Fullerton, CA

3d • Onsite

About The Position

Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not simply valued – they’re invaluable. Join our team at Providence Medical Foundation and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

Requirements

• Completion of an accredited Medical or Phlebotomy training program, or equivalent educ/experience
• College Degree (for department SJuHMG Clinical Trials)
• Phlebotomy Certificate (for department SJuHMG Clinical Trials)
• Bilingual English/Spanish communication skills
• 2 years experience in a Clinical Research setting.

Nice To Haves

• Graduate of a Vocational School or college.
• Biohazardous Material packaging training.
• 3 years preferred experience in a Clinical Research setting.

Responsibilities

• Oversees the day to day functions of multiple clinical research studies.
• Interfaces with the Principal Investigator, Patient, Sponsor, and the IRB.
• Ensures that all documentation is timely and accurate.
• Works closely with the PI to ensure strict compliance to study protocols (GCP/ICH).

Benefits

• Best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree