Jose Trevejo
Chief Medical Officer Enveda Biosciences
Seminars
Thursday 5th November 2026
Standardizing Global Clinical Trial Conduct to Reduce Operational Variability & Improve Cross-Regional Data Reliability
2:00 pm
- Addressing inconsistencies in investigator assessment, adverse event reporting and site conduct across global trial regions, improving operational standardization, to strengthen confidence in safety and efficacy comparisons across multinational studies
- Enhancing site training, oversight and endpoint execution in inflammatory disease trials, reducing investigator-dependent variability and reporting bias, to improve reproducibility across expanding global trial networks
- Balancing increasingly complex biomarker and mechanistic data collection with site and patient burden, streamlining operational workflows and sample logistics, to maintain scalable, executable and regulator-ready study designs
