Job Description
The Clinical Research Associate (CRA) will monitor the progress of clinical studies 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. The CRA implements and monitors clinical trials to ensure sponsor and investigator obligations are met and compliant with local regulatory requirements and ICH-GCP guidelines. They will also assess potential investigative sites, initiate, instruct, and close clinical trials, reviewing and verifying the accuracy of data collected, either onsite or remotely.
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization providing outsourced services to pharmaceutical, biotechnology, and medical device companies.