ICON seeks a Global Study Manager to oversee clinical trial operations across multiple European locations. The role involves managing day-to-day trial activities, coordinating cross-functional teams, ensuring regulatory compliance, and building investigator relationships in a sponsor-dedicated model.
Responsibilities
Plan and manage all aspects of clinical trials within timelines, budget, and quality standards
Collaborate with cross-functional teams to establish and implement trial protocols and procedures
Build and maintain relationships with trial investigators and key stakeholders
Ensure compliance with local, national, and international regulations and ethical guidelines
Identify and resolve critical issues related to trial design, vendor selection, and risk management
Requirements
University degree in medicine, science, or equivalent education and professional experience
Demonstrated ability to drive clinical study deliverables and timelines
Subject matter expertise in assigned therapeutic area
ICON Strategic Solutions seeks a Global Study Manager to oversee clinical trial design, protocol implementation, and regulatory compliance in a sponsor-dedicated role across EMEA. The position involves cross-functional collaboration, data analysis, and stakeholder management to advance therapeutic development. Responsibilities ...
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