Bristol Myers Squibb is seeking a Document Specialist in Warsaw, Poland, responsible for managing regulatory documents and ensuring submission readiness. The role emphasizes collaboration, organizational skills, and proficiency in document management systems
Job Summary
This role facilitates the structure management, submission-readiness formatting, and publishing of critical regulatory documents including clinical study reports and investigator brochures.
The position requires proficiency in electronic document management systems like PRISM and CARA to assemble and remediate externally authored files for eCTD compliance.
Bristol Myers Squibb offers competitive benefits, flexible work environments, and opportunities to grow alongside high-achieving teams transforming patients' lives through science.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking a Document Specialist in Warsaw, Poland, responsible for managing regulatory documents and ensuring submission readiness. The role emphasizes collaboration, organizational skills, and proficiency in document management systems.
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
BS/BA degree with 1-2 years experience
eCTD compliant regulatory document formatting
Proficiency in PRISM/CARA systems
Experience with Word template macros
Acrobat and ISI toolbox usage
Nice-to-have
Strong organizational and communication skills
Ability to work in a matrix team environment
Experience with ICH non-data driven appendices
Key Requirements
Minimum BS/BA degree required
1-2 years regulatory documentation experience
Proficiency in desktop applications and document workflows