Senior Clinical Research Coordinator

Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Senior Clinical Research Coordinator with extensive clinical trial experience. The Senior CRC will work as a primary coordinator on Phase I-III clinical trials in Neurology, Psychiatry, and Cardiometabolic. Candidates should have extensive experience with study start-up, trial execution, adverse event reporting, source creation and documentation, pharmacy and lab operations, as well as query resolutions. Candidates should also have clinical leadership capabilities to serve as an operations leader and train staff as needed.

Job Duties • Coordinate the day-to-day clinical operations of clinical research studies

• Perform study procedures in accordance with GCP and study protocols

• Organize and maintain paper and electronic study data in a complete and correct manner

• Work closely with recruitment and prescreening teams to meet study enrollment goals

• Conduct diagnostic, efficacy, and safety assessments as needed

• Mentor and lead less experienced coordinators and/or research assistants

• Take ownership of team productivity (enrollment) and quality metrics

• Own study study start-up tasks, including vendor communication and qualification

Job Requirements • Five (5) or more years of industry-sponsored drug trial experience

• Demonstrated ability to work on high-enrolling Phase II/III clinical trials

• 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