AbbVie

2021 Experiential Internship - Regulatory Information Management Data Analyst

Employer
AbbVie
Location
Irvine, CA, United States
Posted
Feb 10, 2021
Ref
2102058
Required Education
Bachelors Degree
Position Type
Full time
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .

Purpose :

The Senior Analyst, Regulatory Affairs Registration and Label Management develops strategies, creates and maintains product registration in source system(s). Responsible for reports, metrics,

trending analysis and verification of registration and label management data.

Responsibilities :
  • Creates, maintains and develops strategy for population of meta data and documents in our Registration and
  • Label Management systems such BRIDGE (Building Regulatory Intelligence & Dossiers for Global Excellence)
  • Develops queries, reports and metrics.
  • Able to troubleshoot errors and system performance issues. Works with IT and/or vendor on business problem resolution and enhancements.
  • Participates and contributes in group, department and cross-functional meetings.
  • Interacts with all areas of regulatory affairs and affiliates to ensure registration and label management information is current, accurate and available in regulatory systems.
  • Develops and executes business processes.
  • May have responsibilities for direct report employees or oversight of contract personnel. May indirectly manage the work of other department members.


Qualifications

Minimum Qualifications:
  • Minimum GPA = 3.0/4.0
  • Returning to university for at least one semester and graduating within one-year post internship
  • Currently enrolled in university, pursuing a Bachelor's degree with a major Data Analytics, Information Technology & Systems, Pre-Law or other related field
  • Must be authorized to work in the US on a permanent basis without requiring sponsorship
  • - 3 years pharmaceutical or industry related experience.

Preferred Qualificatoins:
  • Bachelor's degree, RAC certification, PharmD
  • Experience working in a complex and matrix environment.
  • Strong communication skills both oral and written.
  • Experience/understanding/use of software tools.
  • Keen awareness to cultural nuances; proven ability to work in a global environment
  • Strong attention to detail and problem solving skills.
  • Ability to successfully interact with multi-divisional and multi-functional teams from across the globe.
  • Experience in Regulatory Affairs preferred but may consider QA, R&D/support,
  • Scientific affairs, operations or related area. Proven leadership skills in a multi-disciplinary environment and presence.

Note: Higher education may compensate for years of experience

Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
No
Job Type
Internship
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.