Employer Industry: Biotechnology and Pharmaceuticals

Why consider this job opportunity: Salary up to $185,000 per year Eligible for short-term and long-term incentive programs Comprehensive benefits suite, including medical, dental, vision, and prescription coverage Opportunity for career advancement and growth within the organization Flexible work environment with remote options available Unique company culture focused on innovation, diversity, and making a difference in patients' lives What to Expect (Job Responsibilities): Oversee end-to-end case safety management activities for the global commercial product portfolio Ensure compliance with global regulations and guidelines for safety data collection, management, and reporting Act as the main point of contact for internal stakeholders and vendors regarding case handling safety processes Develop and provide training materials for adverse effect collection and reporting Manage inspections and audits related to case processing activities, ensuring compliance and addressing findings What is Required (Qualifications): Bachelor’s degree in nursing, chemistry, biology, or a related field 12+ years of experience in pharmacovigilance in end-to-end case processing of ICSRs with a bachelor's degree, or 10+ years with a master's, or 7+ years with a PhD/PharmD/MD/DO Previous experience using safety databases, preferably Argus Strong written and verbal communication skills Project management skills and ability to organize and deliver large, complex projects independently How to Stand Out (Preferred Qualifications): Master’s degree in chemistry, biology, or a related field 5+ years of experience in vendor management and oversight 3+ years of product development and/or postmarketing drug experience 2+ years of previous functional lead/people management experience Prior pharmacovigilance management experience

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