Description
A field-based Clinical Research Associate will lead clinical trial sites from start-up through close-out in the United Kingdom, supporting investigators and site staff, managing regulatory submissions and study supplies, conducting remote and onsite monitoring, reviewing source data, tracking serious adverse events, maintaining eTMF and CTMS records, and preparing for audits and inspections. The role requires a related bachelor's degree, ICH-GCP knowledge, experience with cell and gene therapies and late-phase clinical trial monitoring, and the ability to travel nationally or internationally.
