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.
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 trials support
Essential document management
Nice-to-have
High-achieving teams rich in diversity
Balance and flexibility in work environment
Cross-functional, multi-cultural teams
Adaptability in complex work environment
Key Requirements
Minimum 3 years of relevant clinical development & operational experience
Bachelor's degree in legal, Life science, Business Administration, or equivalent
Seasoned field monitor with min 3+ years of global site monitoring report review experience is preferred
Prior therapeutic area expertise is preferred
Hands-on experience preparing, reviewing, and submitting regulatory documentation
Hands-on experience of preparing, reviewing, and submitting clinical study start-up / activation documentation