Accredo by Evernorth

LPN Adverse Drug Event Nurse - Accredo - Work from Home, Anywhere, USA

Posted on

March 2, 2025

Job Type

Full-Time

Role Type

Clinical Operations

License

LPN/LVN

State License

Florida

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Company Description

Evernorth Health Services, a division of The Cigna Group, creates pharmacy, care and benefit solutions to improve health and increase vitality. We relentlessly innovate to make the prediction, prevention and treatment of illness and disease more accessible to millions of people. Join us in driving growth and improving lives.

Job Description

Under the direction /supervision of an RN: The Adverse Drug Event Nurse LPN is responsible for completing and submitting adverse drug event reports to the pharmaceutical companies or FDA, following the internal protocols within the nurse scope of practice. Schedule: M-F 10:30-7:00pm EST (09:30-6p CST)

Requirements

Formal Education and/or Training: Practical nursing degree Years of Experience: 0-2 years experience in a clinical setting Licensures/Certifications: Clear, active, unrestricted LPN Nursing license in your home state. Obtain additional state LPN Nurse Licensure as required. Computer or Other Skills: General PC knowledge including Microsoft Office, Internet and email Knowledge and Abilities: Knowledge of pharmacy, pharmaceuticals, or healthcare business required; Works effectively across organization and fosters teamwork; Demonstrates the ability to manage production efficiently while building strong credible working relationships with clients, patients and internal partners; Excellent communication skills both verbal and written; Demonstrated knowledge of medical terminology; Active professional affiliations and/or national certification in related clinical specialty preferred; Ability to work flexible work schedule If you will be working at home occasionally or permanently, the internet connection must be obtained through a cable broadband or fiber optic internet service provider with speeds of at least 10Mbps download/5Mbps upload.

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Responsibilities

Review clinical adverse event “work in progress” (WIP). Use internal protocols to determine if the event should be submitted per manufacturer /FDA requirements. Responsible for accurate documentation of the event to ensure all contractual /FDA requirements are met. Respond to manufacturer and/or internal requests when an adverse clarification is required. Responsible for tracking of these requests as well as other errors identified and notifying the leadership team accordingly. Ensure all applicable manufacturer trainings are completed on time and remain compliant. Attend manufacturer audits as required by the leadership team. 5 % Responsible for good housekeeping techniques, adhering to quality and production standards while complying with all applicable company, state and federal safety and environmental programs and procedures.

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