CMC Regulatory - Clinical Submissions - Belgium

Oct 12, 2016
Nov 11, 2016
Annelies Baere
Organization Type
Contract Type
Full Time

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 or call me on +32 2 403 49 80.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.

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