i3 Drug Safety provides comprehensive pharmacoepidemiology and pharmacovigilance services. Rooted in scientific rigor, using innovative methods and proven expertise, i3 Drug Safety's services can be customized for all scopes of work, from safety surveillance and risk assessment in clinical development to post-approval pharmacovigilance. As a UnitedHealth Group company, i3 Drug Safety is part of a worldwide health care service organization that uses innovation, integrity and commitment to prepare for the future - and you can prepare for yours with us. It's a rare combination for success that only a career with i3 Drug Safety can provide.
We are currently recruiting for Contract Pharmacovigilance Coordinators to work in our Ann Arbor, MI office.
We are seeking highly organized team players to help us review adverse event reports reported to marketed prescription products in compliance with strict regulatory guidelines. This is a fast-paced environment that offers an ideal introduction to the pharmaceutical research industry and a great way to use your clinical skills outside of a direct-care setting. As the Drug Safety Coordinator, you would also enjoy high visibility within the company, a close-knit team, and plentiful growth opportunities.
Responsibilities include:
- Review of adverse event reports, which could include review of medical records
- Data entry into safety database
- Development of a narrative summarizing the patient's adverse events as reported
- Pursuit of follow-up information via telephone or written format
- Compliance with strict reporting timeframes to ensure adherence to international and domestic regulations
- Interaction with team and Project Leader
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