Job Description

Riverside Clinical is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer’s Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer’s Disease.
In this role, we are seeking CRCs with proven trial experience. Ideally, candidates will have worked as a primary coordinator on complex drug trial and have exceeded enrollment targets while producing quality work. Furthermore, we are seeking a bilingual (Spanish) professional to better serve our community.

Job Duties

• Manage daily operations for assigned clinical trial projects
• Perform study procedures in accordance with GCP and study protocols
• Organize and maintain study data in a complete and correct manner in CRIO eSource/CTMS
• Cultivate enthusiastic and professional relationships with patients and sponsors alike
• Work closely with recruitment and prescreening teams to meet study enrollment goals
• Conduct diagnostic, efficacy, and safety assessments as needed

Job Requirements

• Bachelor's degree or higher
• One (1) or more years of clinical research coordinator experience
• Attention to detail and the ability to handle multiple tasks with precision
• Demonstrated ability to work accurately and quickly with CTMS and eSource
• A command of professional spoken and written English
• A command of professional spoken and written Spanish