Senior Safety Data Scientist

Added
1 day ago
Type
Full time
Salary
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Related skills

risk management clinical trials pharmacovigilance regulatory safety data

πŸ“‹ Description

  • Partner with stakeholders to support product safety profile, benefit risk, and signal management
  • Perform standard surveillance of safety data from trials, databases, and literature.
  • Collaborate with safety/clinical teams on signal assessments and regulatory requests.
  • Analyze data to support signal assessment with supervision.
  • Communicate surveillance findings to inform risk minimization and labeling.
  • Prepare safety sections for Clinical OSRs, CSRs, and risk management plans.

🎯 Requirements

  • Degree in Health Sciences (PharmD, MPH, PhD) or Masters with relevant safety experience
  • Knowledge of drug development and regulatory submission processes
  • Familiarity with safety data evaluation tools and SOPs
  • Strong oral/written communication; manage multiple projects
  • Microsoft Word/Excel and basic project management skills
  • Ability to work independently under supervision

🎁 Benefits

  • AbbVie comprehensive benefits package
  • Paid time off, medical/dental/vision insurance
  • 401(k) and long-term incentive programs
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