Global Study Manager
23 ore fa
Genova, Liguria, Italia
Icon Clinical PLC
Tempo pieno
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Overview As a Clinical Trial Manager II at ICON, you design and oversee trials and analyze complex data to advance innovative therapies. You work with cross-functional teams to shape study protocols, enrollments, and day-to-day trial operations while ensuring regulatory compliance and high-quality deliverables. You report on trends and insights to optimize outcomes and tackle challenges with proactive solutions. This role sits at the core of ICON's sponsor-dedicated model, contributing to patient-focused research on a global scale. Retribuzione / Benefits
* competitive base salary
* performance related incentives
* health, dental, and vision coverage
* retirement and pension plans
* life assurance and disability coverage
* employee assistance programmes and wellbeing resources Responsabilità
* Oversee clinical trial management workstreams to meet quality and timeline expectations
* Collaborate with cross-functional teams to design and implement trial enrollment strategies
* Develop and implement comprehensive clinical trial protocols
* Manage day-to-day trial operations ensuring regulatory compliance
* Analyze and interpret trial data to identify trends and optimize outcomes
* Proactively address challenges with effective solutions for successful trial execution
* Communicate with internal and external stakeholders to build partnerships and smooth processes Requisiti fondamentali
* Bachelor's degree in a relevant field
* minimum of X years of experience in clinical trial management
* Proven expertise in designing and executing clinical trials
* Strong understanding of regulatory requirements
* Exceptional analytical and problem-solving skills
* Effective communication and interpersonal skills
* Detail-oriented and highly organized
* Willingness to travel ~25%
* collaboration
* strong communication
* problem-solving
* clinical trial design and execution
* data interpretation and analysis
* regulatory knowledge and compliance
* competitive base salary
* performance related incentives
* health, dental, and vision coverage
* retirement and pension plans
* life assurance and disability coverage
* employee assistance programmes and wellbeing resources Responsabilità
* Oversee clinical trial management workstreams to meet quality and timeline expectations
* Collaborate with cross-functional teams to design and implement trial enrollment strategies
* Develop and implement comprehensive clinical trial protocols
* Manage day-to-day trial operations ensuring regulatory compliance
* Analyze and interpret trial data to identify trends and optimize outcomes
* Proactively address challenges with effective solutions for successful trial execution
* Communicate with internal and external stakeholders to build partnerships and smooth processes Requisiti fondamentali
* Bachelor's degree in a relevant field
* minimum of X years of experience in clinical trial management
* Proven expertise in designing and executing clinical trials
* Strong understanding of regulatory requirements
* Exceptional analytical and problem-solving skills
* Effective communication and interpersonal skills
* Detail-oriented and highly organized
* Willingness to travel ~25%
* collaboration
* strong communication
* problem-solving
* clinical trial design and execution
* data interpretation and analysis
* regulatory knowledge and compliance