Regulatory Affairs Specialist Freelance in Hungary
Requirements:
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0.8-1 FTE based in Hungary (Office in Budapest).
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Medical or Pharmacy educational background + experience with similar responsibilities + fluent Hungarian and English.
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It is temporary solution for 3-6 months with a possibility to extend the partnership further.
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Project starts - 1st of September.
Main Responsibilities:
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Person mainly oriented on promotional materials approval (in Hungarian language for HU and English language for the rest of the markets), medical trainings and providing scientific support / consultations to Commercial team.
Job description:
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*Provide medical and technical training support about Sponsor products and competitors for both LOCs.
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Represent Sponsor in all interactions with consumers, physicians, medical societies, institutions and government bodies.
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With oversight from CEE Area Medical Affairs Lead responsible for medical activities including but not limited to:
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Development and medical approval of accurate, technically supported and business-oriented claims.
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Support to market information / global insights on data collection and analysis of clients products and competitors.
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Coordinating evaluation and approval where required of promotional materials.
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Partner with Pharmacovigilance team in order to ensure that Sponsors activities are conducted in accordance with applicable law and Company policies.
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With oversight from CEE Area Medical Affairs Lead provide medical input to local regulatory applications and new product development.
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Other tasks to support the Sponsors Medical Governance Framework as assigned by CEE Area Medical Affairs Lead.
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Support implementation of scientific engagement activities.
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Product categories: over the counter drugs, medical dvices, cosmetics, food supplements.