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RM
Research Minded
Clinical Research Coordinator
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What they do
A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.
$135,054 / year median in California
+16% projected growth
Job Description
Clinical Research Coordinator Research Minded Roseville, CA Job Details Part-time | Full-time $27 - $33 an hour 4 hours ago Qualifications FDA submissions Filing Microsoft Office ICH guidelines Driver's License Bachelor's degree Communication with regulatory authorities for clinical trials Clinical quality assurance standards Ethical review application preparation Arts Full Job Description Clinical Research Coordinator — Sacramento, CA Area Posted on behalf of a Research Minded client Research Minded is assisting a multi-therapeutic site management organization (SMO) in its search for an experienced Clinical Research Coordinator (CRC) to join its Sacramento-area team. This is a direct-hire position with our client — not a Research Minded position. About the Role The CRC will conduct clinical trials in accordance with Good Clinical Practice (GCP) under the direction of the Principal Investigator and Research Manager, supporting studies across multiple therapeutic areas within the organization's site network. This role is central to protecting human subjects and ensuring studies run compliantly from start-up through close-out. Key Responsibilities Complete FDA and IRB documentation, including new submissions and amendments Conduct the informed consent process and pre-screen patients for protocol eligibility Coordinate subject recruitment, visits, and day-to-day patient care Prepare and maintain case report forms (CRFs) and regulatory binders (paper and electronic) Monitor and report adverse events to investigators and the study team Support study budgeting, billing reconciliation, and sponsor reporting Participate in site initiation visits, monitoring/auditing visits, and investigator meetings Requirements 1-2 years of clinical research experience, including IRB submissions (new and amendments) Working knowledge of federal, state, and local clinical trial regulations, ICH, and GCP Strong MS Office and general computer skills Bachelor's degree in Science or Arts in Sciences preferred ACRP/SoCRA (or equivalent) certification preferred but not required Current BCLS certification preferred Valid driver's license and auto insurance required (travel to physician offices/hospital locations)