Job Description
As a Clinical Research Associate at ICON, you will work within a large‑scale, fast‑paced environment alongside a close‑knit team of highly qualified CRAs to identify, select, initiate, and close‑out investigational sites for clinical studies in phases II‑IV, ensuring adherence to applicable regulations and principles of ICH‑GCP.
Role- Coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation.
- Submit protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required.
- Balance sponsor‑generated queries efficiently and manage study cost‑effectiveness.
- Depending on level of experience, assist in training and mentoring less expert CRAs and/or lead CRAs working on international projects.