What are the responsibilities and job description for the Clinical Research Coordinator (Experienced) position at Irvine Clinical Research?
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. Most of our research is in neurology (Alzheimer's Disease treatment and prevention studies); we also conduct trials in psychiatry and obesity medicine.
In this role, we are seeking CRCs with proven trial experience. Ideally, candidates will have worked as a primary coordinator on a high-enrolling and/or highly complex drug trial and produced quality work.
\n- Manage daily operations for assigned clinical trial projects
- Perform study procedures in accordance with GCP and study protocols
- Organize and maintain paper and electronic study data in a complete and correct manner
- 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
- Two (2) 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
- A command of professional spoken and written English
$66,560 - $80,000 a year
Hours and Compensation
This is a full-time employment position based in-person at our clinic in the Alzheimer’s Orange County building in Irvine or at one of our other network sites in Los Angeles and Riverside Counties. Training will be at our flagship site in Irvine.
The estimated salary for this position is between $66.5k-$80k per year, depending on experience and education.
The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.
\n
Salary : $66,560 - $80,000