Job Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team at ICON plc.
What you will be doing
- Conducting site qualification, initiation, monitoring, and close‑out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high‑quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
Profile
- Bachelor’s degree in a scientific or healthcare‑related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.
- Strong organisational and communication skills, ...