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 / 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
- xugodme 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
- Integral Employee Assistance Programme LifeWorks
- Life assurance
- Flexible country-specific benefits