Description
The Clinical Research Coordinator II coordinates and administers multiple concurrent clinical trials, serving as the primary sponsor contact and coordinating with investigators, study teams, sponsors, CROs, and quality assurance personnel. Responsibilities include subject eligibility and scheduling, protocol documentation, adverse-event reporting, laboratory specimen handling, quality audits, and protocol procedures such as vital-signs collection and electrocardiograms. The role requires a life-science degree or equivalent experience, at least three years of clinical-trial coordination experience, strong communication and organizational skills, Microsoft Office proficiency, and bilingual Spanish-English ability where applicable. The position pays $27.00 to $32.00 per hour.
