Description
Bristol Myers Squibb is hiring a Clinical Research Associate to oversee the quality, integrity, and compliance of clinical trial sites across all trial phases. The role involves site qualification, initiation, monitoring, close-out, data verification, risk assessment, regulatory compliance, vendor/site relationship management, and support for database lock and site closure activities. The position requires a bachelor’s degree, 2–3 years of relevant clinical research experience, knowledge of ICH/GCP and local regulations, strong analytical and communication skills, and proficiency with clinical systems such as CTMS, eTMF, EDC, and RBM tools. The job is remote-based (#LI-Remote) and associated with Bristol Myers Squibb’s clinical development operations.
