Manager, DVM Global Pharmacovigilance Product Surveillance
Zoetis

Job Info

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Role Description

Job Summary:

The position of Global Pharmacovigilance Manager will support global animal health 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. Responsibilities include owning deliverables and embracing priorities that align with promoting patient safety, effective data analysis, and cross-functional communication and collaboration.

Job Responsibilities:

• Post-marketing product surveillance to include but not limited to proactive product monitoring, adverse event trending, signal detection and signal management.
• Provide risk assessments when applicable.
• Represent Pharmacovigilance in cross-functional product surveillance teams
• Author safety review sections of regulatory reports or other communication when required
• Build and maintain technical files within the global signal management system
• Utilize technical tools with the Pharmacovigilance suite of software solutions
• Provide innovative ideas and solutions to evolving signal detection and signal management landscape
• Educate and train others on Global Pharmacovigilance Systems, Processes, and Procedures as applicable.

Experience and Background:

• DVM degree and/or other advanced degree (MS, MPH, PhD) in science such as Biology, Epidemiology, Toxicology, Pharmacy, or related science is required.
• Minimum 5 years' clinical veterinary practice or animal health experience. Large Animal Veterinary experience a plus.
• Experience with pharmacovigilance Signal Detection/Signal Management, data analytics, statistics, and/or epidemiology preferred.
• Knowledge of veterinary Pharmacovigilance regulations across multiple geographies preferred.
• Experience in preparation of regulatory submissions preferred.
• Experience in interpretation of regulations, guidelines, and policies preferred.

Technical Skills Requirements:

• Curious, self-starter with a strong interest in data analysis and patient safety
• Pragmatic and agile, with mature business acumen
• Proficiency in adapting to a dynamic global regulatory environment.
• Aptitude for assimilating data from multiple sources to identify trends and draw scientifically valid conclusions.
• Collaborative partner to build and leverage cross-functional relationships to bring together ideas, data, and insights to ensure proper management of product safety or efficacy issues.
• Highly effective team player and communicator
• Problem solver with an ability to take ownership for issues and have the ability to suggest opportunities for continuous improvement.
• Consistently model behaviors of accountability and ownership through approachability, excellent interpersonal, communication, negotiation, and problem-solving skills.
• High level of competency using Microsoft Office suite - with demonstrated high level competence of working in Microsoft Word and Excel.
• Must be able to effectively communicate in English with colleagues at all levels of the organization and external regulatory agencies.
• Ability to work independently, while fostering good working relationships across physical distance and have flexibility and the capacity to handle multiple tasks at once.
• Attention to detail is critical to ensure that the expectations of all submissions to external agencies are met.
• He/she will be able to influence without authority and support colleagues outside of Pharmacovigilance as the need arises.

Full time

Regular

Colleague

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