Clinical Research Coordinator

One of our top clients, UCLA Health , is looking for a Clinical Research Coordinator to join their on-site team in Westwood, CA 90024. This person will be supporting the company's HIV Trials team, ensuring the proper and timely reporting of research data collected on various research studies as well as other administrative tasks. This includes reporting of research data to the sponsor and to the IRB through their EMR system. This position ensures that the collection and submission of data to sponsoring agencies meet all protocol requirements. This role assists in quality control and quality assurance activities to maintain 'audit-ready' status. We offer a benefits package, which includes enrollable medical, dental, and vision coverage, as well as flexible spending accounts, 401(k) Savings Plans, and employee assistance programs. This is a 6-month contract-to-permanent hire and the team fully intends to onboard this person at the conclusion of the contract. If you are interested in a long-term role that will offer opportunity for expanded growth, please reply as soon as you can! Required Skills & Experience Bachelor's Degree in a relevant field 2+ years of Clinical Research Coordination experience Experience managing clinical research data in a EDC system (such as oncore, recap, medidata) Strong patient facing experience managing patient visits Ability to work with a sensitive population Interventional drug trial experience Experience communicating with sponsors Knowledge of regulatory practices Nice to Have Skills & Experience Epic experience (source documentation) IRB submissions experience Academic institution experience because regulations align