Descripción de la oferta
Experteer Overview As Senior CRA, you will oversee clinical trial monitoring to ensure protocol adherence, regulatory compliance, and high data quality. You will lead monitoring activities with a focus on quality and continuous improvement within a global clinical development context. You’ll work with cross-functional teams to ensure timely data capture and trial execution, and mentor site staff to uphold best practices. This role offers the opportunity to influence trial performance, drive compliance, and contribute to ICON’s mission of shaping the future of clinical development. You will engage with diverse stakeholders and travel up to 60% to sites, enabling impactful, hands-on leadership.Compensaciones / Beneficios
- Monitor sites for protocol, regulatory, and GCP adherence
- Conduct site visits to evaluate performance and resolve issues
- Collaborate with cross-functional teams to ensure timely data collection and reporting
- Provide training and guidance to site staff and other CRAs
- Build and maintain relationships with site personnel and stakeholders to support trial operationsResponsabilidades
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate with strong regulatory knowledge
- Proven ability to manage multiple sites and projects with solid organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management with proficiency in clinical trial software/tools
- Excellent communication, interpersonal, and stakeholder management skills with the ability to drive compliance
- Willingness to travel approximately 60%Requisitos principales
- annual leave entitlements
- health insurance offerings
- retirement planning offerings
- Global Employee Assistance Programme LifeWorks
- life assurance
- flexible country-specific optional benefits
