Drug Safety Reporting Specialist
$55,000–$58,000 year
HybridElk Grove Village, Illinois, United States
Job Summary
Complete adverse event and product quality complaint forms daily to comply with manufacturer reporting requirements. Assist with investigations of adverse events and respond to follow-up inquiries from manufacturers regarding submitted reports. Perform weekly, monthly, and quarterly reconciliation of adverse event and product complaint data as required. Gather information from medical records and patient notes to ensure accurate documentation and timely submission of all reports. Maintain meticulous attention to detail when prioritizing and managing time-sensitive tasks to meet strict deadlines.
Required Qualifications
- Prior experience with Adverse event and product quality complaint reporting
- Ability to gather information from medical records and patient notes and enter into adverse event and product complaint forms that meet manufacturer requirements
- Proficiency with Microsoft products, including Word, Excel, and Power Point, as well as Adobe Acrobat
- Ability to prioritize, multi-task, and manage very time sensitive tasks effectively to meet strict deadlines
- High degree of accuracy and attention to detail
- Excellent written and verbal communication skills
- Pro-active with good analytical skills and problem-solving ability
- Self-directed individual with ability to work independently with minimal supervision
- Ability to work collaboratively and productively with co-workers across the organization
- Familiarity with pharmacy industry and/or previous pharmacy experience
Desired Qualifications
- Prior experience with Adverse event and product quality complaint reporting preferred
- Familiarity with pharmacy industry and/or previous pharmacy experience preferred
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