Consider joining Lancaster Laboratories where people are the most important element in our chemistry. Celebrating 50 years of service, Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. The position will contribute to a Global Pharmacovigilance team s\with the collective responsibilities of addressing post marketing product surveillance of an assigned product portfolio. Post-marketing product surveillance scope will include proactive product monitoring, adverse event trending, signal detection and signal management. The position will require a specialized knowledge of animal health, in addition to regulatory requirements related to signal management, epidemiological principles, and appropriate data analysis methods. This position is expected to carry out work with limited supervision and apply technical knowledge to complete work independently. This position will ensure deliverables and embracing priorities that align with promoting patient safety, effective data analysis, and cross-functional communication and collaboration. Essential duties are not limited to those described below: 1. Provide risk assessments when applicable. 2. Represent Pharmacovigilance in cross-functional product surveillance teams. 3. Author safety review sections of regulatory reports or other communication when required, including but not limited to EU Annual Statements. 4. Build and maintain technical files within the global signal management system. 5. Utilize technical tools with the Pharmacovigilance suite of software solutions. 6. Provide innovative ideas and solutions to evolving signal detection and signal management landscape. 7. Educate and train others on Global Pharmacovigilance Systems, Processes, and Procedures as applicable. 8. Author regulatory submissions associated with signal management activities, when assigned. 9. Provide regulatory guidance and documentation to icRAMS, when requested. 10. Provide regulatory input and appropriate follow-up for inspections, and internal audits and/or process reviews 11. Lead sub-teams within when assigned, to analyze processes, identify problems, and develop effective solutions/strategies Degree in veterinary medicine (DVM), or other related advanced degree. 1. Minimum 3 years' clinical veterinary practice or animal health experience, or similar experience in animal health 2. Experience with pharmacovigilance Signal Detection/Signal Management, data analytics, statistics, and/or epidemiology, preparation of regulatory submissions, interpretation of regulations, guidelines, and policies preferred. 3. Strong verbal and written communication skills, time management and organizational skills, and a demonstrated ability to work in a team environment. 4. Knowledge and understanding of global veterinary pharmacovigilance regulations. 5. Experience with risk management planning 6. Management experience strongly preferred * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays * Career Development and continuing education opportunities Position is full-time, 8am - 5pm with occasional overtime required. #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
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