ICON seeks a Integral 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

📌 Global Study Manager (España)
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📍 España