ICON plc

We are looking for motivated CRAs based in the Paris/Ile-de-France area to join our sponsor dedicated CRA team! As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical clients focused on oncology studies.

As a CTA will play a key role in supporting the management and execution of clinical trials by handling a range of administrative and operational tasks. You will contribute to the smooth execution of clinical trials through efficient coordination, documentation, and communication with various stakeholders.

Join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence, as a CRA homebased in France. You will have ownership of investigator sites for assigned studies and be responsible for the successful management of the site right through to close-out. You will also plan and conduct various site visits, develop effective relationships with investigator site staff, and ensure integrity of clinical data.

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 Site Engagment Liaison/Clinical Research Leader is responsible for the management of clinical sites including the site identification and qualification. The role ensures the timely delivery of clinical trial enrollment in accordance with scientific objectives and ensures inspection readiness at all times for assigned therapeutic areas within a region or country.