03 set - Italia
Iqvia
What you'll do
- Lead and develop a small Pharmacovigilance team, providing coaching, mentoring and day-to-day management
- Ensure delivery of high-quality pharmacovigilance and medical information activities
- Act as a key contact for clients and internal stakeholders across multiple projects
- Support regulatory compliance and inspection readiness across PV processes
- Oversee adverse event and safety case management activities
- Contribute to quality management, process improvements and operational excellence initiatives
- Support business growth through client relationship management and proposal activities
- Deliver PV training and guidance to internal and external stakeholders
What we're looking for
- Bachelor's or Master's degree in Life Sciences or a related field
- Significant experience in Pharmacovigilance within a CRO, pharmaceutical or healthcare environment
- Previous people management experience
- Strong knowledge of European pharmacovigilance regulations and processes
- Experience managing client relationships and stakeholder engagement
- Excellent communication skills in English
- Ability to work independently, prioritize effectively and lead teams in a dynamic environment
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accorda
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