Pharmacovigilance Specialist

¡Be part of the future of drug safety at Asphalion! We’re looking for a  Pharmacovigilance Specialist   ready to embrace new challenges in a fast-moving, international environment. If you thrive on precision and want to make a real impact, we’d love to have you on our team!

Main responsibilities:

Perform weekly global/local literature assessments.
Efficiently manage Individual Case Safety Reports (ICSRs), Adverse Events (AEs), and follow-up activities.
Manage cases through the Pharmacovigilance Database and report accurately to European authorities via Eudra Vigilance.
Translate relevant pharmacovigilance information into English and liaise with Spanish Regulatory Authorities.
Provide support to local and EU Qualified Persons for Pharmacovigilance (EUQPPv).
Stay informed about updates in global and local pharmacovigilance regulations.
Oversee the maintenance of the PSMF and Asphalion’s Pharmacovigilance System (SOPs).
Prepare and review PSURs, RMPs, DSURs, and ACOs with attention to detail.
Offer expert medical advice and support Medical Information projects.
Draft and review Pharmacovigilance agreements and provide strategic insights.
Prepare and conduct internal Pharmacovigilance training sessions.

If you’re passionate about ensuring drug safety and eager to grow professionally, join us at Asphalion and be part of a team at the forefront of pharmacovigilance innovation!

Requirements:
+2 years experience in Pharmacovigilance departments.
Fluent in English & Spanish
Advanced IT level – (MS Office)
Academic Degree in Life Science and Pharmacovigilance.
Proactive, good communication, accurate, detail orientated, teamwork

Why working at Asphalion?
️Permanent contract.
Flexible working schedule - Friday until 15.30h.
Home office & Hybrid or Remote Model  (You can be located anywhere in Spain!)
⚙️ Wide variety of projects, new challenges and experiences.
↗️ Training and personal development program.
English lessons.