Global Study Manager en España

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
• Prior clinical trial monitoring experience preferred
• Willingness to travel approximately 25% as required
• Legal right to work in the assigned country