This role plays a key part in driving the end-to-end execution of clinical trials to ensure they are delivered on time, on budget, and to the highest quality standards
Job Summary
This role plays a key part in driving the end-to-end execution of clinical trials to ensure they are delivered on time, on budget, and to the highest quality standards.
Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue goals both at work and in personal lives.
The position requires managing critical study documentation, vendor oversight, and CTMS milestones while partnering with the Global Trial Lead and key stakeholders.
Matching Summary
This role plays a key part in driving the end-to-end execution of clinical trials to ensure they are delivered on time, on budget, and to the highest quality standards.
Salary
Base: zł180,200 - zł218,360; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs offered
Skills & Requirements
Must-have
Global Trial Management System experience
Clinical Trial Master File systems knowledge
ICH/GCP regulatory guidelines understanding
Vendor invoice processing and accruals
Cross-functional team collaboration
Nice-to-have
Willingness to challenge the status quo
Proactive risk identification and mitigation
Flexible response to changing business demands
Global clinical research experience
Strong oral and written communication skills
Key Requirements
BA/BSc or associate degree in relevant discipline
2-4 years of experience with Clinical Trial Management Systems