Senior Safety Specialist

We are recruiting a Senior Safety Specialist to lead adverse event reporting and pharmacovigilance activities in a regulated environment. Oversee data management, regulatory compliance, and project implementation. Ideal for experienced professionals with expertise in safety reporting and pharmacovigilance.

Skills

• pharmacovigilance
• drug coding software
• meddra
• electronic data capture
• case review
• regulatory reporting
• database management
• quality events management
• clinical trial support
• endpoint assessment
• safety management plan
• project implementation
• mentoring
• budget oversight
• audit preparation
• stakeholder collaboration
• client interaction
• peer report review
• medical terminology
• clinical data reconciliation
• process improvement
• financial monitoring tools