About this role
About the Role Senior CRA at ICON will oversee and manage clinical trial monitoring activities to ensure trials are conducted in accordance with protocol, regulatory requirements, and Good Clinical Practice (GCP) standards. What You'll Do
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
- Conduct site visits to assess site performance, resolve issues, and provide support for successful trial execution.
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
- Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations. What We're Looking For
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- Extensive experience as a Clinical Research Associate with strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills with the ability to influence and drive compliance in a complex environment.
- Willingness to travel as required (approximately 60%). Compensation & Benefits
- Competitive salary and a range of benefits designed to support well-being and work-life balance.
- Annual leave entitlements and health insurance offerings.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme LifeWorks with 24-hour access to a global network of professionals.
- Life assurance and flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, gym memberships, travel passes, health assessments).