Description
The Senior Clinical Research Associate (Level I) will monitor and manage clinical trial sites through remote and on-site visits, assess protocol and regulatory compliance, review documentation and investigational products, conduct root-cause analysis, and escalate and resolve deficiencies. The role also tracks trial progress, supports investigator selection and site initiation, conducts file reviews, responds to audits and inspections, and maintains administrative records. It requires a life sciences-related bachelor's degree or equivalent nursing qualification, at least two years of clinical research monitoring experience, a valid driver's license where applicable, and frequent travel to clinical sites.
