Clinical Research Coordinator

At UCLA Health, you make it happen as part of a groundbreaking Research team, working to understand hundreds of medical disorders and improving processes for dozens of procedures across the globe.

JOB DUTIES JOB QUALIFICATIONS Description The Department of Medicine and Division of Cardiology is seeking a detailed and dynamic Clinical Research Coordinator.

In this role, you will coordinate research studies, identify participants, and assist the Principal Investigator (PI) with patient eligibility.

Responsibilities also include facilitating the informed consent process, educating participants about protocol requirements, and emphasizing the significance of protocol compliance.

The role requires maintaining all necessary documentation in accordance with FDA regulations, Good Clinical Practice (GCP) guidelines, and the funding source.

This includes managing patient registration, data, and treatment assignment.

This role will involve quality control and assurance activities related to study workflows and documentation.

In addition, the Clinical Research Coordinator is responsible for procuring and distributing study supplies, including coordinating specimen collection and shipping.

Ensuring the safe and accurate completion of protocol-required procedures according to regulatory guidelines, FDA CFR, GCP, and institutional best practices is essential.

Hourly range: $32.65-$52.53 DR.

ISLA GARRAWAY UCLA has incredible resources and a team science approach.

The ability to work with collaborative teams and access the amazing resources around campus is the best part about being at UCLA.

RADU UCLA is very diverse in its personnel as well as its many research fields studied SEE WHAT WE'RE UP TO UCLA Health Disability Accommodation Resources Privacy Practices Fraud Alert Sitemap Terms of Use EE/AA Employer ©2024 UC Regents Go to Top