Clinical Research Associate
About the Job
Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. As a Clinical Research Associate at Excelya, you will be responsible for overseeing the progress of clinical trials, ensuring compliance with regulatory requirements, and supporting site staff in their efforts to conduct research that improves patient outcomes.
Main Responsibilities:
- Conduct site initiation visits, monitoring visits, and close-out visits.
- Ensure site compliance with study protocols, ICH-GCP guidelines, and applicable regulations.
- Communicate effectively with study sites to facilitate the trial process and address any issues that arise.
- Review and verify study-related documents and data for accuracy and completeness.
- Monitor patient safety and data integrity throughout the study.
- Assist in preparing for audits and regulatory inspections.
- Provide regular updates to project managers and stakeholders about site progress and challenges.
Requirements
About You: