Job Title:
Drug Safety Specialist Location:
Madrid, Spain (Full-time, On-site) Contract:
6-month contract, Start ASAP Language:
Fluent Spanish required Overview We are looking for an experienced
Drug Safety Specialist
(5–10 years in pharmacovigilance) to support our EU QPPV in post-marketing safety activities.
This is a 6-month contract role based in Madrid, with an immediate start.
Key Responsibilities Oversee pharmacovigilance vendors and partners Maintain the Quality Management System (QMS) and Pharmacovigilance System Master File (PSMF) Draft and contribute to aggregate safety reports (e.g., PSURs) Support local affiliates with PV compliance Manage pharmacovigilance agreements (PVAs) Work within the Argus safety database Requirements 5–10 years' PV experience, mainly post-marketing Strong knowledge of EU PV regulations and GVP Fluent in Spanish and proficient in English Experience with Argus safety system Available to start immediately in Madrid