CMC Regulatory - Clinical Submissions - Belgium
A biotech company is looking for a Clinical Regulatory Affairs Associate to manage the day-to-day support activities to obtain and maintain regulatory approvals for the products, with primary focus on clinical submissions. You will coordinate the CMC part and make sure the documents are prepared to present them to international health authorities. In that way you can expand your network and have a global impact.
- Scientific Degree
- Minimum 3 years of regulatory experience in the pharmaceutical/biotech industry
- Good knowledge of international regulatory affairs regulations (FDA, EMA,…)
- Hands on regulatory experience: IMPD, IND, CMC,…
- Manage multiple projects at the same time
- Fluency in English required, any other language is an advantage
The company is specialized in the discovery and development of small molecule medicines with a big pipeline. This means that is the perfect time to join the company and be involved from the start, control the process and see the results of your hard work. Even more the products are innovative which makes it more interesting and challenging for you.
If this job appeals to you please send me, Annelies De Baere, your most recent CV in Word format to email@example.com or call me on +32 2 403 49 80.
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