AbbVie, Sr. Manager, Compliance (R&D)

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Post Date

  February 15, 2018

Closing Date


LPEC Preferred




Chicago, Illinois



The Sr. Manager, R & D Compliance, will provide direct oversight for moderate to complex elements of AbbVie’s compliance program at the therapeutic area, business unit, functional or corporate level.


Key Job Responsibilities:

  • The Senior Manager will perform the following with minimal to moderate supervision from Ethics and Compliance Officer:
    • Partners with all levels of business functions (including Global RD, HEOR, and Global Medical Affairs) to provide moderate to complex OEC and functional policy interpretation and provide guidance on the requirements. Primary areas of focus include:
      • Clinical Development/Research
      • Global Medical initiatives and programs
      • HEOR initiatives, including Real-World Evidence
    • Provides guidance on proposed business strategies and programs, identifies moderate to complex legal and regulatory issues, analyzes alternatives and works with legal and other functions, as appropriate, to propose solutions to the business.
    • Develops model and conducts compliance risk assessments, trend analysis and provides recommendations for compliant business activities.
    • Provides strategic insight to development of KPIs/metrics relating to relevant compliance areas
    • Conducts moderate to complex policy and procedure reviews and updates related to OEC policy and functional procedures ensuring clarity, applicability and compliance.
    • Develops, delivers and updates OEC’ s comprehensive training program on moderate to complex OEC and functional policies and procedures,
    • Develops, implements, modifies, and oversees corporate and/or functional monitoring plans and any corrective actions to ensure compliance with policies and procedures.
    • Assists ECO on compliance audits, when necessary, such as overseeing the fulfillment of auditors’ requests and acting as a liaison between the business and auditors during on site activities.  Expected to evaluate and help respond to moderate to complex preliminary audit findings and recommendations, and to guide the business in preparing corrective action(s) to address moderate to complex findings and recommendations, and work with the business to ensure timely completion.
  • Participates in and may lead moderate to complex cross-functional OEC programs.

Supervisory Responsibilities:

  • May have direct reports with people management responsibility.

Key Leadership Competencies:

  • Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance
  • Learns, fast, grasps the 'essence' and can change the course quickly where indicated
  • Raises the bar and is never satisfied with the status quo



Minimum Education:

  • BA/BS required.  CPA, Master's, JD, or equivalent work experience preferred.

Minimum Experience:

  • Minimum of 7 year's experience with, or exposure to, business functions such as compliance, legal, regulatory affairs, government affairs, and finance.
  • Preferred: experience providing compliance support in pharma/biopharma or medical device industry


Equal Opportunity Employer Minorities/Women/Veterans/Disabled



Apply Online

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