Global Trial Acceleration Associate

Roles & Responsibilities:

• Execute centralized activities for global clinical trials
• Coordinate with CROs, Country Trial Managers, CTMs, CRAs, and study teams
• Manage essential documents, ethics committee submissions, and regulatory files
• Support study start-up activities including site activation and documentation
• Review and maintain clinical systems such as CTMS, eTMF, and Veeva Vault
• Oversee outsourcing, contracting, translation, and investigator file setup
• Ensure quality control and compliance with ICH-GCP and internal standards
• Act as primary point of contact for centralized trial start-up and maintenance activities

Qualification:

• Bachelor’s degree in Life Sciences, Legal, or Business Administration
• Advanced degree preferred

Experience:

• 3+ years of experience in clinical development or clinical operations
• Experience in pharma, biotech, or CRO environments
• Hands-on experience in IRB / IEC submissions and site activation

Skills:

• Strong knowledge of ICH-GCP and global regulatory documentation
• Proficiency in CTMS, eTMF, Veeva Vault, MS Office, and SharePoint
• Excellent organizational, communication, and coordination skills
• Strong attention to detail and decision-making ability
• Therapeutic area exposure (Oncology, Cardiology, Immunology) is a plus

About the Company:

Bristol Myers Squibb is a leading global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines that transform patients’ lives through science.