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