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 Saint John's 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. Phlebotomy Certificate upon hire (for department SJuHMG Clinical Trials) F02 AMG Clinical Trials: Required to have College Degree 2 years of experience in a Clinical Research setting. 3 years preferred.

Why Join Providence?

Our best-in-class benefits are 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.

Accepting a new position at another facility that is part of the Providence family of organizations may change your current benefits. Changes in benefits, including paid time-off, happen for various reasons. These reasons can include changes of Legal Employer, FTE, Union, location, time-off plan policies, availability of health and welfare benefit plan offerings, and other various reasons.