Experteer Overview 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 / Beneficios
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 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 Adaptable country-specific benefits