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# PV Associate Analytics & Reporting

- **Company:** Galderma SA
- **Location:** Barcelona, Spain
- **Contract:** Permanent contract
- **Skills:** Data Analysis, Databases
- **Published:** October 17, 2026
- **Apply:** https://galderma.wd3.myworkdayjobs.com/External/job/Barcelona/PV-Associate-Analytics---Reporting_JR021148-1

## About the Role

* Degree in Pharmacy or another relevant scientific discipline, with at least five years of experience in life sciences.
 * Significant experience in pharmacovigilance, particularly post-marketing safety activities at a global or headquarters level.
 * Strong knowledge of post-marketing pharmacovigilance regulations for medicinal products, with an understanding of relevant cosmetics regulations and industry best practices.
 * Extensive experience in aggregate reporting, risk management methodologies and signal detection for medicinal products.
 * Experience collaborating with external service providers, local affiliates and cross-functional stakeholders.
 * Strong analytical skills, attention to detail and the ability to manage multiple activities and deadlines.
 * Excellent written and spoken English.

## Description

We are looking for a Global PV Associate - Analytics & Reporting to support pharmacovigilance activities for our global portfolio of marketed medicinal and cosmetic products, ensuring patient safety, regulatory compliance and effective post-marketing safety surveillance., * Perform routine global pharmacovigilance activities, including aggregate reporting, signal detection and management, literature monitoring, and risk management.

 * Lead and coordinate the preparation and review of aggregate safety reports, ensuring scientific quality, accuracy and compliance with applicable regulations and timelines.
 * Provide scientific oversight of external pharmacovigilance service providers.
 * Support regulatory submissions, marketing authorisation maintenance and responses to requests from health authorities.
 * Contribute as a subject matter expert to upgrades and improvements of pharmacovigilance databases and tools.
 * Prepare and maintain departmental quality documents, support process improvements and contribute to operational excellence., * The opportunity to contribute to global pharmacovigilance activities within a leading dermatology company.
 * An international and collaborative working environment.
 * Opportunities to develop your expertise and contribute to continuous improvement and operational excellence.
 * The chance to make a meaningful impact on product safety and patient well-being.

Next Steps

Our recruitment process typically includes an initial conversation with Talent Acquisition, an interview with the Hiring Manager and further discussions with relevant stakeholders.