Senior Clinical Research Associate (Site Monitor II)

About the role

Join Excelya, where audacity, care, and energy define how we work. This role offers an exciting opportunity to contribute to a dynamic, ambitious Clinical Operations team. You will play a critical part in driving innovation and making an impact in the clinical research space.

Key responsibilities

• Ensure regulatory, ICH‑GCP, and protocol compliance at sites.
• Evaluate site and staff performance, recommend actions, and develop escalation plans.
• Conduct source‑document review and verification of medical records.
• Manage reporting of protocol deviations and follow‑up actions.
• Enter observations into tracking systems and monitor adverse‑event queries.
• Perform on‑site and remote monitoring activities in line with country regulations.

Required profile

• Minimum 3 years of clinical monitoring experience in oncology.
• Bachelor’s degree or equivalent in a related scientific field.
• Fluency in Greek and English.
• Willingness to travel for site visits.

What we offer

• High‑impact projects that drive innovation in patient care.
• Opportunities for personal and professional growth in an inclusive environment.
• A collaborative culture that values audacity, care, and energy.