
Support the operational execution of global clinical trials, ensuring activities are completed on time and in compliance with ICH-GCP, regulatory requirements, and company procedures. Coordinate study logistics, documentation, systems updates, and trial-related tracking activities. Maintain oversight of study records, including (e)TMF management and archiving readiness. Collaborate with cross-functional teams and external partners to support efficient study conduct. Identify operational risks, quality issues, or delays and escalate as appropriate. Contribute to process improvements, training, inspections, audits, and maintenance of procedural documents. Perform other clinical trial administration and operational support activities as assigned.