This individual contributor role has task-level responsibility for clinical trial related document collection, compilation, review and approval across all phases of global clinical trials
Job Summary
This individual contributor role has task-level responsibility for clinical trial related document collection, compilation, review and approval across all phases of global clinical trials.
The Global Trial Acceleration Associate will interact with clinical study sites, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitor (CTMo.), the study team and other functional areas within BMS and will provide support to the Study Team throughout the study duration.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer 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.
Matching Summary
This individual contributor role has task-level responsibility for clinical trial related document collection, compilation, review and approval across all phases of global clinical trials.
Skills & Requirements
Must-have
Clinical trial document collection
Site Monitoring Visit report review
ICH/GCP and regulatory guidelines
Global clinical trial documentation
Stakeholder relationship management
Nice-to-have
Therapeutic area expertise
Cross-functional team collaboration
Adaptability in complex environments
High performance in changing environments
Key Requirements
Minimum 3 years clinical development experience
Bachelor's degree in legal, Life science, Business