Senior Global Trial Acceleration Associate

The Senior Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation. They will interact with clinical study sites, Central/Local IRB/IECs, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitor (CTMo.), the study team and other functional areas within BMS and will provide support to the Study Team throughout the study duration (start-up, maintenance, and close-out of clinical studies).

Requirements

• Minimum of a bachelor’s degree in legal, Life science, Business Administration, or equivalent experience.
• 3-5 years of relevant clinical development & operational experience in Pharmaceutical, biotech, CRO or similar fields, is required.
• Hands-on experience preparing, reviewing, and submitting regulatory documentation to IRB/IECs and Regulatory Agencies; including formulating responses to queries.
• Hands-on experience of preparing, reviewing, and submitting clinical study start-up / activation documentation, including responses to queries.

Benefits

• Competitive benefits
• Services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.