
Detail-oriented clinical operations professional with strong scientific knowledge and hands on experience supporting global clinical studies from start-up through conduct and close oversight. Skilled in coordinating study activities, maintaining trial systems and documentation, and developing trackers, dashboards, and timelines that improve visibility and keep projects on schedule. Known for collaborating effectively with study managers and cross-functional teams to support compliant, inspection-ready trial execution, while proactively identifying risks, resolving issues, and contributing to high-quality study delivery.
Management:
Technical:
(SCQF level 6 -3 Credit points)
- Project Management Foundations: Budgets
Abstracts: