$188,250 - $228,114; not specified; not specified ...
Hybrid (50% onsite)
Global risk-based gcp audit strategy
Vendor quality oversight framework
Third-party risk management (tprm)
Bristol Myers Squibb is seeking a Director of Audit Strategy and Vendor Quality to lead the design and execution of a global audit strategy ensuring compliance with Good Clinical Practice. The ideal candidate will have extensive experience in quality assurance within clinical development, strong leadership skills, and a proven ability to drive vendor quality oversight
Job Summary
The Director, GCP Audit Strategy and Vendor Quality is accountable for designing and executing a global, risk-based audit strategy to ensure compliance with Good Clinical Practice (GCP) requirements.
This role will drive robust vendor quality oversight across all clinical trial service providers in close partnership with Development Quality.
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
Match Score: 85
Bristol Myers Squibb is seeking a Director of Audit Strategy and Vendor Quality to lead the design and execution of a global audit strategy ensuring compliance with Good Clinical Practice. The ideal candidate will have extensive experience in quality assurance within clinical development, strong leadership skills, and a proven ability to drive vendor quality oversight.
Salary
$188,250 - $228,114; Not specified; Not specified
Skills & Requirements
Must-have
global risk-based GCP audit strategy
vendor quality oversight framework
Third-Party Risk Management (TPRM)
ICH/GCP and global regulatory requirements
Health Authority inspections
Nice-to-have
Quality by Design principles
predictive analytics
automation and efficiencies
transformative mindset
external landscape assessment
Key Requirements
12+ years in Quality Assurance or regulated clinical development
Proven leadership of global audit strategy
Demonstrated experience with Health Authority inspections
Direct involvement in M&A, in-licensing, and due diligence
B.S. or M.S. in a scientific, health, IT, or quality-related discipline