Site Activation Partner

As a Site Activation Partner you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions. You will be a dedicated resource to one of ICON's clients, embedded in their working environment, systems, and processes. Your responsibilities will include collecting, preparing, reviewing, approving, processing, and tracking regulatory and site-level critical documents required for study site activation in accordance with ICON's SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines, and the principles of ICH/GCP. You will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of treatments and therapies. The role requires a Bachelor's degree in life sciences or a related field along with experience in clinical research and regulatory submissions, specifically with local ethics submissions in Argentina (FEFYM) and Provincial committees. Fluency in Spanish and advanced English is also essential.