Clinical Safety Analyst

Added
1 hour ago
Type
Full time
Salary
Salary not provided

Related skills

clinical trials ich pharmacovigilance ema fda

πŸ“‹ Description

  • Support world-wide surveillance of clinical trial patient safety data.
  • Contribute to continuous process improvement and cross-functional teamwork.
  • Assist in safety data review and ad-hoc safety reports as needed.
  • Collaborate with medical monitor and clinical teams on study safety reviews.
  • Maintain audit readiness for study deliverables.

🎯 Requirements

  • Bachelor's degree with health science background; RN or clinical pharmacy experience preferred.
  • At least 2 years clinical practice experience; 1 year drug safety in clinical trials preferred.
  • Proficiency with Windows/Office and databases (e.g., Oracle/clinical, PIMS).
  • Ability to critically evaluate medical data and ensure regulatory compliance.
  • Effective communication; fluent in Japanese and business-level English.

🎁 Benefits

  • AbbVie benefits package; opportunity for career growth.
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