Global Trial Acceleration Associate in Hyderabad, भारत

Bristol Myers Squibb seeks a Global Trial Acceleration Associate to manage centralized clinical documentation and regulatory activities supporting global clinical trials. The role involves coordinating with study sites, vendors, and internal teams across trial start-up, maintenance, and close-out phases.

Responsibilities

• Manage essential document handling, regulatory submissions, and ethical compliance activities
• Coordinate with clinical sites, CROs, and country trial managers throughout study lifecycle
• Initiate and manage start-up documentation and site activation processes for global trials
• Review site monitoring visit reports, escalate issues, and track resolution and follow-up tasks
• Maintain and update clinical trial management systems to report document status and trial progress

Requirements

• Bachelor's degree in law, life science, business administration, or equivalent experience
• Minimum 3 years clinical development and operational experience in pharma, biotech, or CRO
• Hands-on experience preparing and submitting regulatory documentation to IRBs and agencies
• Knowledge of ICH/GCP guidelines and clinical study activation procedures
• Proficiency in CTMS systems, MS Office, SharePoint, and clinical trial technologies
• Strong stakeholder management and cross-functional team collaboration skills
• Fluent English communication (written and oral) with excellent organizational abilities