Fluent in English/Spanish required. Must be able to run a study from start to finish. Conduct eligibility screening interviews over the phone and/or in person. Schedule study patient appointments and make reminder calls to patients: send reminder letters and emails as appropriate. Conduct study patient visits per protocol, including screening and follow-up visits, data collection and entry into Case Report Form (CRF), specimen collection, processing, shipping in accordance to IATA requirements, and other study activities. Ensure that all Serious Adverse Events (SAEs) are reported in a timely fashion to IRB and sponsor. Responsible for maintaining various site logs (i.e. Site visit logs, study subject enrollment logs, screening logs, drug accountability logs). May be asked to attend Investigator Meetings for new trials as assigned.

Required Experience:

Must have working experience as a CRC. Ability to multi-task. Working understanding of ICH, GCP and FDA regulatory requirements. Excellent verbal, written and organizational skills. Ability to work independently. Flexible work hours (Mon-Fri). Strong team player.

Work Location:

In person