Description of job position
- Preparing, submitting, and implementing registration documents of pharmaceutical products.
- Ensuring the correct translation and comprehensibility of technical texts shown on the packaging and package inserts of medicines.
- Negotiation with the company’s internal clients.
- Communicating with regulatory authorities, state institutions (National Institute for Drug Control, Ministry of Health of the Slovak Republic) and the company's headquarters.
- Preparing, submitting, and detailed processing of requests for the authorisation of clinical trials.
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Position Regulatory Affairs Manager - Medicine & Social Care in the labour market
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