Senior Clinical Research Associate - Remote - FSP

Join our diverse and dynamic team as a Clinical Research Associate at ICON, where you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. This role is fully sponsor dedicated and you would be working in an FSP model. Within this program you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client, you will experience a true “one team” approach that provides limitless opportunity to develop through training, mentorship, and support from leadership. You will be conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. You will collaborate with investigators and site staff to facilitate smooth study conduct as well as perform data review and resolution of queries to maintain high-quality clinical data. You will also contribute to the preparation and review of study documentation, including protocols and clinical study reports.