Global Study Manager en Madrid, España

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

• Collaborate with cross-functional teams to design and implement clinical trial enrollment strategies
• Develop and implement comprehensive clinical trial protocols
• Oversee day-to-day clinical trial operations and ensure regulatory compliance
• Analyze clinical trial data, identify trends, and provide insights to optimize outcomes
• Communicate with internal and external stakeholders to support trial execution

Requirements

• Bachelor's degree in relevant field
• Minimum 5 years global clinical trial management experience
• Expertise in clinical trial design and execution
• Strong understanding of regulatory requirements
• Analytical and problem-solving skills with medical data interpretation ability
• Effective communication and cross-team collaboration skills
• Detail-oriented with ability to manage multiple priorities