Bristol Myers Squibb is seeking a Document Specialist in Warsaw, Poland, to manage regulatory documentation and ensure submission readiness. The role involves collaboration with internal and external teams, requiring proficiency in document management systems and regulatory processes
Job Summary
This role facilitates the structure management and submission-ready formatting of critical regulatory documents including clinical study reports and investigator brochures.
The position requires partnering with internal teams and external authors to assemble documents using PRISM, CARA, and Core Template workflows.
Bristol Myers Squibb offers a wide variety of competitive benefits and programs designed to support employees in pursuing their goals both at work and in personal lives.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking a Document Specialist in Warsaw, Poland, to manage regulatory documentation and ensure submission readiness. The role involves collaboration with internal and external teams, requiring proficiency in document management systems and regulatory processes.
Salary
Base: zł144,100 - zł174,616; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs provided
Skills & Requirements
Must-have
eCTD compliant regulatory documents
PRISM/CARA electronic systems
Word template macros proficiency
Acrobat and ISI toolbox usage
Clinical study report formatting
Nice-to-have
Strong organizational skills
Matrix team collaboration
Cross-functional communication
Timeline management abilities
Key Requirements
Minimum BS/BA degree required
1-2 years regulatory documentation experience
Proficiency in electronic document management systems