[Hiring] Pharmacovigilance Specialist I @Mindlance

Role Description

Monitor and report any adverse events or side effects of pharmaceutical products on the market. Report adverse reactions and product complaints received from healthcare professionals and consumers.

• Responsible for collecting, monitoring, processing, and distributing adverse event reports and information queries.
• Prepare and submit adverse event cases to pharma clients or FDA.
• Reviews safety and medical information for the assigned products, including safety components of protocols and studies for assigned drugs.
• Prepares and mails time-sensitive documentation necessary for the processing of adverse event cases.

Qualifications

• High school diploma or equivalent.
• Associate’s degree preferred.
• 1+ years of pharmaceutical or healthcare related work experience.
• Medical assistance or project coordination experience preferred.
• Experience or basic knowledge of adverse events preferred.
• Proficient with Microsoft Office Suite (Outlook, Word, Excel).

Requirements

• Training is 4-8 weeks, most time spent shadowing a team member on actual tasks.
• User will process AE documents each day based on assignments from shared excel log.
• Performance expectation is completion of 33 reports per 8-hour day.

Benefits

• Equal Opportunity Employer: Mindlance does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.