Experteer Overview
La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación.
In this role you will lead clinical trial start-up activities to enable timely site activation while ensuring regulatory compliance. You will work with cross-functional teams to streamline processes, guide study teams and sites, and advance start-up strategies. The position challenges you to manage multiple projects in a fast-paced environment and stay up-to-date with industry regulations. This role offers a meaningful impact on how ICON delivers efficient, compliant trials at scale.
Compensaciones / Incentivos
• Lead preparation and submission of regulatory documents for approvals and site activation
• Coordinate with cross-functional teams to streamline study start-up processes
• Oversee/site identification and selection to meet project criteria and compliance
• Provide guidance and support to study teams and sites during start-up
• Stay current with regulations and trends to enhance start-up strategies
Responsabilidades
• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience in study start-up activities with regulatory knowledge
• Experience managing multiple projects and prioritizing in a fast-paced environment
• Excellent organizational skills and attention to detail
• xqbhyrx Strong communication and interpersonal skills for collaboration with diverse stakeholders
• Commitment to high standards of quality and compliance
• Willingness to travel approximately 15%
Requisitos principales
• Annual leave entitlements
• Health insurance offerings
• Competitive retirement planning
• Global Employee Assistance Programme LifeWorks
• Life assurance
• Flexible country-specific benefits