Quality Assistance 1

CDMXICON plc is a world-leading healthcare intelligence and clinical research organization.
We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.What You Will DoTrial Documentation & eTMF Management Oversee clinical trial documentation, including CTA packages for Health Authority (HA) and Ethics Committee (EC) submissions.Maintain and ensure compliance of the electronic Trial Master File (eTMF), including timely uploads, quality checks, and archiving at study closeout.Support investigator TMF setup and documentation completeness.Quality Oversight & Compliance Perform compliance checks and process reviews across clinical study activities (e.G., regulatory, feasibility, study start-up, contracts, and trial management).
Ensure adherence to SOPs, local procedures, and regulatory requirements.Document findings and track follow-up actions to closure.SOP Deviations ...