Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization that drives innovation in clinical development. The company supports patients by accelerating the development of drugs and devices that save lives and improve quality of life.

Responsibilities

As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

Qualifications

• Bachelor’s degree or international equivalent in a scientific or health‑related field or equivalent combination of education and clinical research experience, especially in a study coordinator or nursing role.
• 1+ years of clinical monitoring experience (level2) or 3+ years (level3). A combination of education a...