Principal Global Trial Associate
Bristol Myers Squibb · Hyderabad, IN
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
What they're looking for
- Experience managing clinical trial documentation and eTMF systems
- Knowledge of ICH/GCP guidelines and regulatory compliance requirements
- Project management skills with ability to handle multiple complex trials
- Strong organizational and prioritization abilities with minimal supervision
- Experience with clinical trial management systems (CTMS) and vendor oversight
- Cross-functional collaboration and communication skills
What you'll be doing
- Execute clinical study operations ensuring compliance with ICH/GCP and regulatory guidelines
- Develop and manage study documentation, timelines, and deliverables across multiple trials
- Support Global Trial Lead in maintaining eTMF accuracy and study completion
- Track performance metrics, identify risks, and implement mitigation strategies
- Manage vendor relationships, country planning, and study closure activities
Privacy & handoff
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