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
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 - ...
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