The Clinical Research Associate I will function under the supervision of the Clinical Research Supervisor, coordinating and maintaining diverse activities related to clinical trials at the John Wayne Cancer Institute. This includes, but is not limited to: patient screening, eligibility, registration, quality control of data compilation and submission, study evaluation, as well as direct patient follow-up by phone. Interacts closely with institutional investigators and industry sponsors. Collaborates with the Clinical Research Nurses throughout study completion. Must uphold the standards of confidentiality, attendance and punctuality.  Performs all duties in a manner, which promotes team concept and reflects the Sisters of Providence mission and philosophy.  

Providence caregivers are not simply valued – they’re invaluable. Join our team at John Wayne Cancer Institute 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: 

Bachelor's Degree Or equivalent educ/experience 1 year Clinical research coordination, or 2 years of clinical research data entry or equivalent experience in Clinical Trials

Preferred Qualifications: 

Upon hire: ACRP or SOCRA certification, or other Clinical Research Certification 1 year experience with Phase I-II trials Oncology experience Experience with Electronic Data Capture systems (InForm, Medidata Rave, etc.)

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.