JOB DESCRIPTION:
Responsible for:
• QA validation of key department outputs
• Continuous improvement initiatives
• Process enhancement initiatives
Purpose
• To assure quality of key outputs of the Global drug safety department including case management, trials support and pharmacovigilance.
• To act as the catalyst for continual improvement initiatives
Outputs
• Quality assured reports and reviews
• Quality performance metrics
• Continuous improvement initiatives
JOB REQUIREMENTS:
Skills/Knowledge Required:
• Minimum of B.S. or the equivalent combination of relevant education or professional experience
• Advance degree preferred
Experience
• Five (5) years relevant experience, including training
• Three (3) years pharmaceutical/biotechnology industry experience
• Drug safety experience
Knowledge
• Expert knowledge of the safety regulatory environment
• Proficiency in technical safety systems including ARISg and medical coding
• Computer and database skills
Competencies
• Attention to detail
• Diplomacy
• Communication (written & oral)
• Organisation and planning
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