-- Receive and process information from various channels, including voice calls for safety reporting.
-- Route safety reports to relevant departments (e.g., Medical, QA).
-- Monitor mailbox, triage patient safety reports, and maintain records.
-- Handle source documents, update shared folders, and enter data per criteria.
-- Obtain consent for follow-ups, assess cases for missing information, and ensure closure.
-- Validate cases, prevent duplicate entries, and address data discrepancies.
-- Enter and evaluate safety information, assess case seriousness, and perform follow-ups.
-- Translate and back-translate safety data as needed.
-- Archive and review source records for missing/discrepant data.
-- Extract and process safety reports from databases/registries.
-- Document reviews, ensure SLA adherence, and maintain data per guidelines.
-- Collaborate with quality teams to enhance case quality.
-- Attend training, develop skills, and mentor new joiners as required.

What you need to have:

-- Graduate in Pharmacy or Life Science
-- 1 year of Pharmacovigilance or relevant clinical experience
-- Excellent spoken and written Dutch and English proficiency

What we offer:

-- Competitive salary and benefit package (cafeteria + annual bonus)
-- Training and continuous learning and certification opportunities
-- Chance to be part of a rapidly expanding organization
-- Multilingual, multicultural environment with native colleagues
-- All You Can Move SportPass (at a discounted price)
-- Free medical benefit package
-- Reimbursable language courses
-- Team events, company events
-- Relocation package
-- High value awards and recognitions