Senior/Principal Study Start-up Specialist Netherlands in Netherlands

Clinical Trial Submission Specialist (Associate - Lead Level) - Netherlands (FULLY REMOTE HOME BASED) - Permanent

Advanced Resource Managers are currently actively looking for Regulatory candidates in the UK to join a leading level CRO within the long standing submission teams. Having placed 12 candidates into their wider team, we are well placed to give you an overview of what it would be like working in this team and development opportunities our client can give you.

Main duties you will be covering are as follows -

· Prepare, review and coordinate, under guidance, local regulatory submissions

· Provide guidance local regulatory strategy advice to various sponsors

· Key-contact at country level for either Ethical or Regulatory submission-related activities

· Working with the clinical team to prepare the regulatory compliance review packages

· Ensure the local country study files and filing processes are prepared

To be considered for this role, you must hold the following -

· Bachelor's degree

· 1 - 5 years clinical experience or equivalent combination of education, training, & experience

· Effective oral and written communication skills

· Excellent interpersonal skills

· Basic knowledge of all applicable regional / national country regulatory guidelines and EC regulation.

If you are interested in hearing more about this opportunity, please email for more details.

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.