Job Description Training, consultation and support of Study Site Coordinators /Research Nurses on clinical studies Providing non-operational site support to ensure progress of clinical study and to ensure that it is conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and the applicable regulatory requirement(s) Notifying Study Monitor / Team on any site issues that are detected in contact with the clinical center and are relevant for them Establishing and maintaining relationships with Study Site Coordinators and Investigators to optimize performance of clinical study Assistance in development of recruitment strategies and tracking of recruitment or patient retention activities at the site