Regulatory Submission Associate (Belgium) in Belgium

Regulatory Submissions Associate - Flexible work style - Belgium - Permanent

Here at ARM, we are actively looking to engage bright candidates who are looking to move into Regulatory Affairs space within the Pharma industry for a large and trusted CRO who have great reputation for their Submissions team in Belgium.

We have a great track record of placing candidates in the past year within the team and we believe that we can provide the support and information about the role. It is a fantastic work environment and various development opportunities that are in place for the candidates made transparent from the start.

Your main duties will be as follows:

• Preparing, reviewing, and coordinating local regulatory and EC submissions
• Maybe a point of contact at country level for Ethical and Regulatory submission-related activities
• Working with start-up CRAs to prepare the regulatory compliance review packages
• Ensure the local country study files and filing processes

Experience needed for this role are as follows:

• Diploma or degree level educated
• Relevant experience OR understanding of clinical trials can be considered (no hands on experience is required)
• Effective language skills in English and Dutch/ French
• Basic understanding of regional/ country level regulatory guidelines and EC regulations

Disclaimer:

This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission.