As a CRA II, you will monitor multiple Phase I, II, III & IV clinical trial sites across different therapeutic areas. The CRA is the main sponsor representative, providing key project updates, collaborating with the team, and developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely. You will review source to CRF/eCRF, ensuring patient safety and data integrity. You will also oversee the sites' adherence to GCP/ICH practices.

This contract position ensures that data collected for clinical studies is accurate, plausible, and traceable to source documentation, assisting in site management, and clinical study materials development.