
Senior Clinical Research Associate/Clinical Research Associate - FSP
The CRA (or Senior CRA) will manage assigned clinical study sites including initiation, monitoring (onsite and remote), SDV/SDR, CRF review, CTMS and eTMF updates, drug accountability, SAE reporting, and preparation for audits/inspections. Requires knowledge of ICH-GCP, relevant local regulations, ability to work remotely, and willingness to travel as required. Bachelor's degree in a related life science discipline is specified.













