Clinical Research Associate Oncology
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About the Job
Excelya invites you to join a team defined by Audacity, Care, and Energy. We foster bold innovation and support a collaborative environment where personal and professional growth thrive.
As a Clinical Research Associate at Excelya, you will be integral to ensuring the successful execution of clinical trials by overseeing site activities, adherence to protocols, and regulatory compliance. This role is pivotal in advancing clinical projects that aim to improve patient care.
Main Responsibilities:
- Conduct site initiation, monitoring, and close-out visits to ensure compliance with clinical trial protocols.
- Maintain effective communication with investigators and site staff to support trial progress.
- Review and verify clinical trial data and documentation for accuracy and completeness.
- Monitor patient safety and data integrity throughout the study duration.
- Assist in preparation for audits and inspections, ensuring sites are inspection-ready.
- Report deviations, adverse events, and other study-related issues in a timely manner.
- Collaborate with project managers to provide updates and address challenges encountered at sites.
Requirements
Requirements: