Clinical Study Lead Phase 2,3 and 4

As a Clinical Study Lead (CSL) you support the Development team in contributing to the clinical evaluation of new drug candidates through the operational management of multinational clinical trials phase 2, 3 and 4. Leading the Clinical Study Team and act as Functional Area Leader for all clinical operations activities from initial study planning, setup and conduct until final reporting phase with overall responsibility to remain within agreed budget, timelines and expected GLPG quality standards.

That means more detailed:

• Appropriate planning of budget, resources and timelines for allocated studies
• Actively initiate and participate in Process Improvement initiatives
• Be responsible to deliver a clinical study from initial planning, setup and study conduct until final reporting phase within agreed budget, timelines and with high quality (comply with GLPG processes, ICH-GCP and applicable regulations and guidelines)
• Initiate and coordinate the vendor selection process
• Be the primary contact person for selected vendors and ensure high quality oversight according to study plans, timelines and budget
• …

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