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Job opportunities for foreign professionals in Sweden!
Gruppchef Saftey/Vigilance till Q-Med
maintenance of device and drug safety database and procedures to enable collection, data entry, medical assessment, reporting, monitoring and trending of adverse event case reports and medical complaints
continuous evaluation of safety for products under clinical development and post- market approval
provide innovation and strategy to develop, implement and enhance vigilance and pharmacovigilance plans including comprehensive risk benefit assessments and risk minimization/management plans to establish and appropriately communicate safety profile of products
convey safety information/messages to internal customers including senior management, subsidiaries, marketing and sales teams and externally to regulatory agencies and government authorities worldwide, key customers, stakeholders and patient community as required.
Qualification in medicine, pharmacy or a relevant scientific discipline.
At least 5 years of management experience in a relevant field, preferably in international vigilance/pharmacovigilance operations.
High level experience in device/drug safety including in-depth knowledge and working compliance experience with worldwide safety regulations.
Understanding of medical and scientific principles associated with administration of products.
High level of technical and ethical expertise.
Experience in writing complex safety/clinical analyses.
Fluency in both English and Swedish.