Case Management Specialist

Job title: Case Management Specialist

Company: Zentiva


Job description: Be a part of the winning culture!At Zentiva, we are a team of 4.700 unique talents bonded together by our common mission. We believe our diversity is a source of great energy and strength, and we create a work culture and ethics where everyone feels appreciated, can be their true selves, and contribute to the best of their ability. Seeking for a balanced team across the company we welcome applications from all qualified candidates with various educational and industry experiences, cultural or ethical backgrounds, and different life experiences or abilities, regardless of their religious or philosophical beliefs or whomever they choose to love.Case Management SpecialistThe successful candidate will be responsible for case processing from case intake, follow-up request, data entry and check to reporting to authorities or business partners. The candidate will work with either German or English case reports and need to communicate follow-up requests in these languages.Your ResponsibilitiesReporting mailbox check.Case reports intake, personal data redaction, translation GEàEN.Duplicity check and data entry.Peer to peer Quality check.Follow-up in English and German.MedDRA coding, listedness and causality evaluation.EudraVigilance triage and import.Reporting to authorities and partners.Monthly and quarterly reconciliations.Documentation of the activities.Any other case management associated matters as defined in GVP Module VI.We RequireUniversity / Bachelor degree preferably in chemistry/natural science/pharmacy.Fluent English (advanced) and German language (intermediate)Sense for details and accuracy, ability to work with minimum supervision and escalate relevant information to management.Computer skills – proficiency with MS Office tools (excel, word, power point), MS Sharepoint, etc.Experience in the fields below can be an advantageOther areas of Pharmacovigilance, Regulatory Affairs in Pharmaceutical Industry.Experience in case management (either clinical or post-marketing) in the sense of GVP module VI.Knowledge of PV Safety database ARISg or EudraVigilance.What is in it for youAn opportunity to work for a successful international pharmaceutical company.An opportunity to learn newest approaches in managing creative and highly adaptive business organizations.Pleasant and dynamic working environment.Continuous personal development.An attractive compensation & benefits package.Above standard social and benefit program.

Expected salary:

Location: Praha 10

Job date: Fri, 25 Jul 2025 22:10:42 GMT

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