Clinical Research Associate 2 - Full Time

The role of a Clinical Research Associate II involves conducting on-site monitoring for clinical trials across various therapeutic areas such as CNS, cardiovascular, obesity, and NASH/MASH. Key responsibilities include site selection, initiation, monitoring, and closeout visits in compliance with GCP and regulatory standards building relationships with investigative sites and providing protocol and study-specific training monitoring study progress, patient recruitment, enrollment, and data queries evaluating site compliance, identifying risks, and preparing monitoring reports collaborating with cross-functional teams and supporting patient recruitment and administrative activities. Qualifications And Skills Bachelor's degree At least 1 year of independent on-site monitoring experience in CRO, biotech, or pharmaceutical settings Knowledge of GCP, ICH, and clinical trial regulations Strong communication, organizational, and problem-solving skills Proficiency in Microsoft Office applications.