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Clinical Research Coordinator at Providence Medical Grp.

Orange, California, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Mar, 26

Salary

0.0

Posted On

03 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Documentation, Compliance, Phlebotomy, GCP, ICH, Patient Interaction, Study Protocols, Biohazardous Material Training, Team Collaboration, Principal Investigator Liaison, Sponsor Communication, IRB Interface, Medical Training, Clinical Trials Management

Industry

Hospitals and Health Care

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. Phlebotomy Certificate (for department SJuHMG Clinical Trials) upon hire. 2 years - 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.

Responsibilities

The Clinical Research Coordinator oversees the day-to-day functions of multiple clinical research studies. This role involves ensuring timely and accurate documentation while maintaining compliance with study protocols.