Clinical Research Associate: Site Monitoring & Compliance Expert

Bristol Myers Squibb is seeking a Clinical Research Associate to serve as the primary site contact, ensuring quality, integrity and compliance of clinical trial activities in line with protocol, SOPs, ICH GCP and regulatory requirements. This role involves coordinating monitoring visits across trial phases and maintaining documentation.

You will train site staff, manage relationships with investigators and vendors, support audits, and help meet study objectives including enrollment and data