Associate Director, Safety Data Sciences

Added
1 day ago
Type
Full time
Salary
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Related skills

pharmacovigilance regulatory submissions microsoft excel microsoft word clinical study reports
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πŸ“‹ Description

  • Lead surveillance activities for products across lifecycle using data from trials, safety
  • Collaborate with safety/clinical teams to plan signal assessments and regulatory requests.
  • Analyze data for signal assessment and prepare materials for ad hoc regulatory safety requests.
  • Communicate safety findings to inform risk minimization and labeling decisions.
  • Prepare and maintain safety sections of Clinical CS, CSRs, CDSS, and Risk Management Plans.

🎯 Requirements

  • Degree in Health Sciences or relevant advanced degree; or equivalent combination of education and
  • Knowledge of drug development, regulatory requirements, and safety science integration.
  • Experience with safety data evaluation methods and cross-functional collaboration.
  • Strong oral/written communication and ability to manage multiple projects.
  • Proficiency in Microsoft Word and Excel; basic project management; independent work capability.

🎁 Benefits

  • AbbVie offers a comprehensive benefits package including PTO, medical/dental/vision, and 401(k).
  • Eligibility for long-term incentive programs; equal opportunity employer commitments.
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