Job Description:

• Completing and submitting adverse drug event reports to the pharmaceutical companies or FDA
• Review clinical adverse event "work in progress" (WIP)
• Respond to manufacturer and/or internal requests when an adverse clarification is required
• Ensure all applicable manufacturer trainings are completed on time and remain compliant
• Attend manufacturer audits as required by the leadership team

Requirements:

• Minimum of 2 years experience in a clinical setting
• Clear, active, unrestricted LPN Nursing license in your home state
• General PC knowledge including Microsoft Office, Internet, and email
• Knowledge of pharmacy, pharmaceuticals, or healthcare business required
• Excellent communication skills both verbal and written
• Demonstrated knowledge of medical terminology
• Active professional affiliations and/or national certification in related clinical specialty preferred

Benefits:

• medical, vision, dental, and well-being and behavioral health programs
• 401(k)
• company paid life insurance
• tuition reimbursement
• a minimum of 18 days of paid time off per year
• paid holidays