Responsibilities Include:

• Selecting and coding adverse events
• Determine seriousness of AEs, writing/editing case narratives
• Perform labeling assessments
• Requesting follow-up information when needed
• Adhere to regulations, guidelines, Standard Operating Procedures, data entry and writing practices

Qualifications:

• Bachelor’s Degree
• 4 to 7 years of experience in Quality Assurance and Quality Control
• HCP is required
• Drug Safety experience is desired