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Peter Van Reusel provides executive leadership to the development and implementation of clinical standards in line with CDISC’s strategy and operational plans, working closely with the President and CEO, as well as CDISC staff and stakeholders. He has over 20 years’ experience in senior roles in pharma and at CROs, providing standards expertise and carrying out other standards work in various organizational settings. A long-time, CDISC-authorized instructor, Peter has helped significantly in developing CDISC training courses.

He previously served as CDISC’s European Liaison, shepherding relationships with key European regulatory, academic, and biopharma stakeholders. Peter is also an active PHUSE working group leader.