Description
The Clinical Operations Analyst will support clinical study activities in R&D, including study planning, contract and statement-of-work preparation, purchase-order and invoice processing, site payment monitoring, budget reconciliations, equipment procurement, inventory and shipment management, device accountability, documentation, reporting, and communication with investigators, site staff, and internal teams. The role requires Microsoft Office proficiency, familiarity with contractual terms, knowledge of the medical, pharmaceutical, or clinical research industry, and strong communication, teamwork, negotiation, and attention-to-detail skills. It is onsite five days per week in Irvine, California, with a stated pay rate of $35 per hour and requires 2–3 years of experience.
