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About AbbVie

AbbVie (NYSE:ABBV) is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions. The company’s mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world.  For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook or LinkedIn.​

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Senior Medical Safety Analyst

Research & Development
1907961 Requisition #
Join our Talent Community


  • Collect, assess and process adverse event information (clinical and post marketing) in a compliant and timely manner in order to comply with global regulations which includes: Seriousness assessment, Labeling, Causality, Initial and Follow up
  • Meeting company standards for quality, compliance and productivity. Remaining current on knowledge and skills required for case processing.
  • Understanding of the changing regulatory environment and the impact to the case management process.
  • Meets case quality, case processing metrics and agility by exhibiting the Abbvie core leadership attributes: Agile and Accountable; Clear and Courageous; Make Possibilities Real; All for One AbbVie; Decide Smart and Sure
  • Supporting and participating in audits and inspections as needed
  • Grows knowledge and expertise to initiate mentoring opportunities of other MSA’s in case processing in their primary area PMS or Clinical.
  • Other duties may be assigned based on the need or work requirement of the organization.

 Position can be hired as a Medical Safety Analyst or Senior Medical Safety Analyst based on the candidate's education and years of experience.


  • Minimum: Bachelor’s degree with related health sciences background, RN, BSN, BS, BS Pharm.
  • Candidates lacking the appropriate degree but with previous pharmaceutical experience may be considered
  • 2-4 year clinical experience or 2-3 years clinical experience and 1 year pharmacovigilance experience.
  • Demonstrated ability to lead project work. Proven success in results-driven process management
  • Core knowledge of industry regulations (ICH, FDA, EMEA, MHRA)
  • Competent in case processing processes, procedures, conventions


Equal Employment Opportunity Employer

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.

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