We are seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities, ensuring adherence to protocol, regulatory requirements, and industry standards. The successful candidate will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
Requirements
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Benefits
- Annual leave entitlements
- Health insurance
- Retirement planning
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits