Sr CRA 1

Job Overview

The Sr Clinical Research Associate (CRA) is responsible for performing high‑quality monitoring activities and site management to ensure that clinical sites conduct studies in full compliance with the protocol, ICH‑GCP guidelines, regulatory requirements, and sponsor expectations. This role plays a key part in safeguarding data integrity, patient safety, and overall study performance.

Essential Functions

• Conduct site monitoring visits (selection, initiation, routine monitoring, and close‑out) in alignment with the contracted scope of work and Good Clinical Practice.
• Partner with sites to develop, adapt, and track recruitment strategies to meet project timelines and enrollment targets.
• Deliver protocol and study‑specific training to site personnel; maintain consistent communication to manage expectations and resolve issues proactively.
• Assess the quality and integrity of site practices, ensuring ad...