Global Trial Acceleration Associate

We are seeking a Global Trial Acceleration Associate to manage and execute centralized activities in support of global trials with an emphasis on clinical documentation. The successful candidate will interact with clinical study sites, CROs/vendors, Country Trial Managers/CTMo, and other functional areas within BMS to provide support to the Study Team throughout the study duration.

Requirements

• Minimum of a bachelor’s degree in legal, Life science, Business Administration, or equivalent experience.
• Minimum 3 years of relevant clinical development & operational experience in Pharmaceutical, biotech, CRO or similar fields, is required.
• Seasoned field monitor with min 3+ years of global site monitoring (Clinical Research Associate) report review experience is preferred.
• Prior therapeutic area expertise (eg: Oncology, Cardiology, Hematology, Immunology etc) is preferred.
• Hands-on experience preparing, reviewing, and submitting regulatory documentation to IRB/IECs and Regulatory Agencies; including formulating responses to queries.
• Effective communication skills in English (written & oral), computer skills - MS office suite, SharePoint, etc. CTMS (Veeva Vault experience preferred, knowledge of portals, databases and other Clinical Trial enabling technologies