Senior Analyst, Regulatory Affairs Registration Management

Employer
AbbVie
Location
Lake County, Illinois, USA
Posted
May 30, 2018
Ref
1803964
Required Education
High School or equivalent
Position Type
Full time
The Senior Analyst Regulatory Affairs Registration Management, is responsible for the development of strategies for the population of information into systems. Expert in country/area assessment of registration data. Responsible for reports, metrics, trending analysis and verification of registration data

Key Responsibilities Include:

  • Develops strategy for population of products/countries for the registration Management area.
  • Develops queries creating reports, metrics, trending analysis, verification of data.
  • Responsible for monitoring area of responsibility for changing regulatory requirements that would impact the system.
  • Works with IT and/or vendor on business problem resolution and enhancements.
  • Interacts with all areas of regulatory affairs and affiliates.
  • Develops and executes business processes for Registration Management.
  • May manage contract employees
Basic:

  • Required Education: High School diploma or equivalent and 9 years of related experience
  • Preferred Education: Bachelor's Degree. Certifications a plus (RAC, PMP, Green/Black belt)
  • Required Experience: 3 years pharmaceutical or industry related experience
  • Experience working in a complex and matrix environment. Good communication skills, both oral and written
  • Preferred Experience: Demonstrated analytical capabilities. Project management experience
  • Proven leadership capabilities in a multi-disciplinary environment
  • Experience/understanding/use of software tools
Note: Higher education may compensate for years of experience. Years of experience may compensate for lower education.