Clinical trial disclosure is typically managed at the jurisdiction level, with teams treating each country’s registration and results-posting obligations as separate, isolated tasks. The “fishing line” approach, managing each requirement individually, may appear efficient on the surface, but can introduce significant risks:
Thomas Wicks
Head of Transparency Operations
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Head of Transparency Operations
Citeline
Thomas Wicks is an experienced strategic leader with over 20 years in life sciences. As Head of Transparency Operations, he spearheads strategy for Citeline's industry-leading disclosure solutions. Thomas is an established thought leader, having spoken at over 60 conferences and authored over 40 publications on disclosure requirements and transparency trends. Thomas is motivated by empowering teams to accelerate solutions that honor trial transparency.
Ben Evans
Disclosure Regulations Research Manager
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Disclosure Regulations Research Manager
Citeline
Benedict Evans is a regulatory professional with expertise in clinical trial disclosure, medical technology, and biotechnology.
As Disclosure Regulations Research Manager at Citeline, Benedict works on the content development and expansion of TrialScope Intelligence, ensuring that sponsors have access to reliable, up-to-date regulatory insights to inform actionable regulatory intelligence. With a strong foundation in science, regulation, and project management, Benedict has worked across the biotech, life sciences, and medical technology sectors, helping organizations navigate regulatory requirements.
