Associate Director Global Pharmacovigilance

Job Summary: We are seeking a dynamic and experienced leader to join our Global Pharmacovigilance (GPV) team as an Associate Director. In this critical role, you will lead a dedicated team responsible for a wide range of pharmacovigilance activities. You will be instrumental in ensuring our operations are compliant, efficient, and consistently meet the highest standards of quality and safety. The ideal candidate will be a strategic thinker with a passion for developing people and driving process excellence.

Lead and manage Global Pharmacovigilance team members, overseeing activities such as case review and approval, aggregate report preparation, and signal management Establish team priorities, allocate resources effectively, and track progress to ensure all timelines and objectives are met Participate as needed in Global PV Leadership team meetings Support and participate in regulatory audits and inspections, including readiness preparation and management of Corrective and Preventive Actions (CAPAs) Responsible for participation in or support/oversight of one or more of the activities described below: Ensure the creation, review, and maintenance of a robust procedure management process for all Global PV documents Support the safety database and other PV IT applications, including participation in business-related tasks such as IT application testing Provide expert support to national PV teams as needed to ensure global alignment and compliance Monitor, interpret, and apply new and existing legislation governing pharmacovigilance to ensure ongoing compliance Oversee a comprehensive training program for GPV staff and other relevant personnel Leadership Expectations: We are looking for a leader who excels in fostering a culture of excellence and growth. The successful candidate will be expected to demonstrate core leadership skills, including: Mentoring & Coaching: Actively manage team questions, facilitate group meetings, and provide guidance to develop the skills and careers of your team members Continuous Learning: Stay current with evolving legislation and maintain a robust training program to ensure your team remains at the forefront of the field Proactive Problem Solving: Engage directly in resolving challenges as they arise and implement effective risk minimization strategies to prevent future issues Continuous Improvement & Innovation: Drive the enhancement of our processes and systems by participating in new projects and consistently seeking opportunities for innovation Required Qualifications: PhD or DVM with 3 years experience in a highly regulated pharmaceutical field; OR Master's degree with 5 years experience in a highly regulated pharmaceutical field Desired Qualifications: Experience with statistical analyses In-depth knowledge of regulations governing pharmacovigilance for veterinary medicinal products Proficiency with pharmacovigilance databases and other IT applications Strong analytical, communication, and writing skills Required Skills: Adaptability, Adverse Event Report, Audit Inspections, Compliance Monitoring, Data Management, Pharmacovigilance, Process Improvements, Regulatory Compliance, Regulatory Reporting, Strategic Planning, Training and Development Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we