Regulatory Affairs Specialist with Clinical Trial Expertise
1 week ago
We are looking for a skilled Regulatory Affairs Specialist to join our team in Hungary. The ideal candidate will have expertise in clinical trials and a strong understanding of regulatory procedures.
About the RoleThis is a unique opportunity to work as part of a multinational company's CRO Partner team, where you will be responsible for coordinating regulatory intelligence procedures and training in allocated countries. You will also be involved in implementing and developing regulatory affairs procedures, supervising local regulatory officers, and ensuring the periodic update of clinical trial regulation files.
The successful candidate will have experience in direct work within the field of regulatory, along with confident IT skills and a professional level of English. This role offers a competitive salary of around €45,000-60,000 per year, depending on experience, plus an annual bonus and benefits such as a welcoming and open team environment, cafeteria, and more.
Key Responsibilities- Taking an active part in the start-up activities of clinical trials
- Coordinating regulatory intelligence procedures and regulatory training in allocated countries
- Implementing and developing regulatory affairs procedures
- Supervising local regulatory officers and ensuring the periodic update of clinical trial regulation files
- University or college degree in medical or clinical research-related discipline, or acceptable combination of education and experience
- One to two years of direct work experience in the field of regulatory
- Confident IT skills and professional level of English
This role offers a range of benefits, including:
- Competitive salary: €45,000-60,000 per year (depending on experience)
- Annual bonus
- Cafeteria
- Welcoming and open team environment
If you are a motivated and experienced regulatory affairs specialist looking for a new challenge, we encourage you to apply for this exciting opportunity. Please send us your fresh CV and we look forward to reviewing it.
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