Found Description
Senior Clinical Research Associate – São Paulo
ICON plc is a world‑leading healthcare intelligence and clinical research organization. As a Senior Clinical Research Associate, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Key Responsibilities
- Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conduct site visits to assess site performance, resolve issues, and provide support to ensure 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 t...
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