Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials)
Reconciliation activities for all types of received reports.
Work under supervision and mentoring of a more experienced colleague.

🎯 Requirements

Life science / biomedical background – healthcare degree (chemistry, biology, biotechnology
Previous experience in Data Entry or QC.
End-to-end case processing experience (2-3 years).
ARGUS/LSMV/ArisG experience required.
Time/issue management, delegation, organization and multitasking with attention to detail.
Strong interpersonal and communication skills.

🎁 Benefits

Training and career development opportunities internally.
Strong emphasis on personal and professional growth.
Friendly, supportive working environment.
Opportunity to work with colleagues worldwide, with English as the company language.
Quality, Integrity & Trust, Drive & Passion, Agility & Responsiveness, Belonging

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