Job Overview As a Remote Site Coordinator, you will be responsible for ensuring that study sites are conducting the trial and reporting data as required by the study protocol, regulations, and sponsor requirements. This role requires strong organizational and problem-solving skills to manage multiple priorities within various clinical trials. 1. Serves as an in-house CRA responsible for site management, data review, and query resolution on assigned projects. 2. Performs study evaluation, initiation, remote monitoring, and close-out visits remotely. 3. Serves as a primary contact between the business and the investigative site and ensures proper documentation of site management communications. 4. Collaborates with field CRAs to resolve and document outstanding site issues/action items. 5. Reviews the quality and integrity of patient data at assigned sites through remote review of electronic case report form (CRF) data. Qualifications 1. Bachelor's Degree in a scientific discipline or healthcare preferred. 2. Minimum of 2 years of clinical experience required. 3. Knowledge of clinical research process and medical terminology. 4. Excellent written and verbal communication skills.