Senior Global Trial Acceleration Associate
LifelancerHyderabad, Telangana, India
Posted March 4, 2026
Full Time
About the Company
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Job Description
Working as a Senior Global Trial Acceleration Associate at Bristol Myers Squibb, you will be responsible for managing and executing centralized activities in support of global trials with an emphasis on clinical documentation. You 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 provide support to the Study Team throughout the study duration (start-up, maintenance, and close-out of clinical studies).
Requirements
- 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
- Hands-on experience preparing, reviewing, and submitting regulatory documentation to IRB/IECs and Regulatory Agencies
- Knowledge of ICH / GCP and regulatory guidelines/directives
- 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
- Proven experience in managing key internal and external stakeholders effectively
Benefits
- Competitive benefits
- Services and programs
- Pursue goals, both at work and in personal lives
