In 2022, the Clinical Development and Clinical Operations tracks have been combined in order to ensure consistency throughout the content development and avoid any overlapping or duplication.

This comprehensive track will cover evolution in clinical operations, data management, interacting with regulators, patient engagement and other important learnings from the past and the latest advances in clinical research.

Who is This Track Designed For?

DIA recommends this track and associated sessions to professionals involved in research and development, evidence generation, protocol development, study design, biomarker development, project management, patient centricity, statistics, clinical regulatory professionals and clinical assessors, clinical operations, and statistics, medical affairs, clinical quality assurance, regulatory affairs, vendor and alliance management and data management. Also for clinical reviewers, clinical research associates, study managers, patient recruitment professionals.

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