Senior Regulatory Officer
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About the role
Hybrid Senior Regulatory Officer role in Prague supporting clinical trial and ethics submissions for medicinal products. Responsibilities include CTIS submissions, regulatory strategy, authority and ethics committee communication, risk mitigation, document review, safety reporting, and training. Requires a college/university degree or equivalent education, training and experience, at least five years of Czech clinical trial submission experience, extensive CTIS experience, and full working proficiency in Czech or Slovak and English.
Key requirements
- • College/University degree or an equivalent combination of education, training and experience
- • At least 5 years of relevant experience
- • Required skills: Clinical trial submissions in the Czech Republic, Clinical Trial Information System (CTIS), Regulatory strategy, Regulatory risk identification and mitigation, Communication with regulatory authorities and ethics committees, Safety reporting to authorities, MS Office applications, Communication, Collaboration, Problem-solving
- • Required languages: Czech or Slovak, English
Opportunity details
- • Workplace: Hybrid
- • Posted: Oct 27, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Senior Regulatory Officer
Location: Prague, Prague, Czechia