Senior CRA
ICON plcParis, Ile-de-France, France
Posted February 24, 2026
Full Time
About the Company
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Job Description
We're 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.
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
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits