Inglewood 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
Equal Opportunity & Fair Chance Employer Irvine Clinical Research and its affiliates are Equal Opportunity Employers. We celebrate diversity and are committed to creating an inclusive environment for all employees.Get more roles like this
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