Global Study Manager
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
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