The Senior Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation
Job Summary
The Senior Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.
Support outsourcing activities by interfacing with operational teams, support groups and service providers for successful selection, contracting and execution of outsourced studies while ensuring compliance with regulatory standards, ethical practices, BMS outsourcing and procurement policies and procedures.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.
Matching Summary
The Senior Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.
Skills & Requirements
Must-have
Clinical documentation management
Regulatory submission support
Site activation
eTMF maintenance
ICH/GCP compliance
Nice-to-have
Cross-functional team collaboration
Adaptability in complex environments
Stakeholder management
Key Requirements
Bachelor's degree in legal, Life science, Business Administration, or equivalent experience
3-5 years of clinical development & operational experience
Experience with regulatory documentation submission
Experience with clinical study start-up/activation documentation