Patient Safety
hace 2 semanas
TASKS :
Management of case forms received in the context of clinical studies, including: Transmission of information to the Global Safety Database.
Management of queries generated from the Global Safety Database with study leaders. Acting as a contact interface for local clinical study managers for Pharmacovigilance issues related to case reporting. Review notifications to ensure compliance with data protection requirements and censor personal data information if applicable. Coordinate translation requests with external vendor and transmit English translation of information received in local language. Ensure reconciliations are performed with the various reporting source interfaces (e.g. Customer Service, Medical Information, QCO, Licensees, etc.) according to established frequencies and archive documentation resulting from reconciliations. Review of incidents and/or inquiries received from the Customer Service department for identification of Pharmacovigilance information and forwarding, if appropriate, to the responsible team (e.g. Medical Information, QCO). Data entry, processing and follow-up management of adverse event case reports under local responsibility.SKILLS :
Experience in Pharmacovigilance Department / with tasks related to Pharmacovigilance (e.g. clinical trials). Bachelor's degree in health sciences or related. Fluent Spanish &English language level B2.
SCHEDULE :
08/09h-17/18h from Monday to Friday (flexible). Hybrid work mode. 50% Teleworking.
CONDITIONS :
Permanent contract. Restaurant ticket on the days you go to the office.
Flexible remuneration plan (free of income tax), we provide you with:
private medical insurance, public transport ticket and childcare vouchers. Discounts in the gym network (Andjoy). Training and development. Referral bonus for referring a person who meets the profile we are looking for. Your recommendation is an extra guarantee of quality
Our goal is for you to be well in every way
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