Clinical Research Coordinator

Providence; Fullerton (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

Providence Medical Foundation is seeking a Clinical Research Coordinator to oversee day-to-day activities across several clinical studies. The role requires collaboration with the Principal Investigator, patients, sponsors, and IRB to ensure protocols are followed and documentation remains timely and accurate.

A strong emphasis exists on GCP/ICH compliance. The ideal candidate has completed an accredited medical or phlebotomy program, with 2 years of clinical research experience preferred and

Qualifications

• Must have completed an accredited Medical or Phlebotomy training program.
• Experience in a Clinical Research setting is preferred (2 years; 3 years preferred).
• Bilingual English/Spanish communication skills are advantageous.

Responsibilities

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

Skills

Bilingual English/Spanish

Clinical communication

Education

Accredited Medical/Phlebotomy training program

College degree

Job description

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.

Required Qualifications:

• Coursework/Training: Completion of an accredited Medical or Phlebotomy training program, or equivalent educ/experience

Preferred Qualifications:

• Graduate of a Vocational School or college.
• Coursework/Training: Biohazardous Material packaging training.
• F02 AMG Clinical Trials: Required to have College Degree
• Upon hire: Phlebotomy Certificate (for department SJuHMG Clinical Trials)
• Bilingual English/Spanish communication skills
• 2 yearsexperience in a Clinical Research setting. 3 years preferred.

Why Join Providence?

Ourbest-in-class benefitsare uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities.