Executive Vice President Pv Operations H/F - 75

We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.

Come and join us in this exciting journey to make a positive impact in patient's lives.The Executive VP, Pharmacovigilance (PV) Operations is responsible for leading and overseeing all operational aspects of global pharmacovigilance activities, ensuring compliance with regulatory requirements, company SOPs, and industry standards. This role will manage PV teams, optimize operational processes, and collaborate cross-functionally to ensure the highest level of patient safety and product quality. They will be focused in ensure we optimizes the cost, speed and quality of delivery through levering metrics to inform management interventions.



Role and Responsibilities

Leadership & Strategy

- Provide strategic direction for PV operations, aligning with corporate goals and regulatory expectations.
- Develop comprehensive operational strategies that align with the company's overall objectives. This involves understanding the long-term goals of the business and creating plans that ensure these goals are met through efficient operational processes.
- Development and implementation of strategic plans for the expansion of the Safety and Pharmacovigilance services in terms of revenue, operational margins and resources
- Lead, mentor, and develop PV operational teams, fostering a culture of accountability, high performance, and continuous learning.
- Partner with the Enterprise PMO/BPO to realize the objectives of the value creation plan (VCP)
- Represent PV operations at senior/executive management meetings, governance boards, and cross-functional leadership forums.
- Accurately forecast future needs and allocate resources accordingly. This includes planning for upcoming projects, ensuring that the necessary resources are available, and optimizing their use to achieve maximum efficiency and productivity.
- Define KPIs and monitor team performance

Operational Excellence

- Champion a culture of excellence across global PV operations, embedding best practices, innovation, and continuous improvement to enhance patient safety outcomes.
- Collaborate with Enterprise PMO/BPO to optimize and standardize end-to-end pharmacovigilance process, ensuring efficient, compliant, and high-quality execution of PV project management, case processing and literature, medical scientific affairs, PV regulatory and PV medical information.
- Optimize operational frameworks by streamlining workflows, leveraging automation, and integrating emerging technologies to improve data accuracy, reporting timeliness, and decision-making speed.
- Identify optional process variation and engage with commercial leadership to ensure we maximize revenue for these options.
- Collaborate with Enterprise PMO/BPO to and monitor KPIs and performance dashboards to proactively track operational efficiency, compliance metrics, and signal detection performance.
- Drive global harmonization of PV processes across regions, affiliates, and partners to ensure consistent execution and regulatory alignment.
- Lead inspection readiness and quality excellence initiatives, ensuring that PV systems, documentation, and processes exceed regulatory expectations and withstand scrutiny from health authorities.
- Foster cross-functional collaboration with Regulatory Affairs, Quality, Medical Affairs, and Clinical Development to integrate safety insights into strategic product lifecycle management.

Process Improvement & Innovation

- Drive operational excellence through process mapping, automation, and technology adoption.
- Evaluate and implement advanced PV tools, AI-supported case processing, and process efficiencies.
- Lead change management initiatives to adapt PV operations to evolving regulatory and organizational needs.
- Partner with the Enterprise PMO to realize the objectives of the value creation plan (VCP)
- Collaborate with Enterprise PMO/BPO to lead the transformation of PV processes through the adoption of automation, advanced analytics, and AI-driven solutions to enhance efficiency, accuracy, and scalability.
- Streamline workflows and eliminate redundancies to optimize resource allocation, reduce cycle times, and strengthen safety data quality.
- Leverage industry benchmarking and best practices to identify and implement process enhancements that drive competitive advantage.
- Implement robust change management strategies to ensure successful integration of new tools, systems, and methodologies across global PV teams and partners.
- Engage with Enterprise PMO/BPO to ensure adherence to corporate governance for the initiation of new and on-going change iniatives.

Cross-Functional Collaboration

- Act as a strategic bridge between Pharmacovigilance Operations and key internal stakeholders, ensuring safety intelligence informs and enhances corporate decision-making across the product lifecycle.
- Embed PV insights into strategic business planning, ensuring that patient safety, compliance, and benefit-risk considerations are central to portfolio management and market expansion decisions.
- Facilitate global alignment by harmonizing safety processes and communications between affiliates, regional offices, and headquarters.
- Contribute to cross-functional governance committees and safety boards, providing expert safety input for product development, launch readiness, and lifecycle management.
- Promote a culture of shared accountability for patient safety, enabling cross-departmental ownership of pharmacovigilance excellence.