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Job Details
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Regulatory & SSU Specialist - fully remote - Belgium

Business Type: Clinical Research Organisation
Job Type: Clinical Research
Job Level: Experienced (non manager)
Position: Full Time
Location: Belgium
Reference: 323415EM BE
Closing Date: 31/05/22
Job Details:

Regulatory & SSU Specialist - fully remote - Belgium

Do you have experience in study start up and want to join a team of the very best who strive to make a difference in the life sciences industry and improve patient health? Our client is looking for a highly motivated Regulatory & Study Start Up Specialist to join their team in Belgium/The Netherlands.

This role is sponsor dedicated; you will only have to deal with one set of protocols and SOPs. This makes the role much more straight forward, easier to manage, and will make your workload more feasible.

Our client is one of the best CROs for career progression and development. Through their tailored training and mentorship programmes, you will have the opportunity to progress to the next step in your career, moving on to CPM or beyond. Whatever your career goals are, they will work to get you there and help you achieve your goals.

The client has offices in Brussels; however the role can be worked fully remote so it is open to candidates from anywhere in Belgium or The Netherlands. The decentralised nature of the role means that there is no need for a long commute or relocation, saving you time and money and giving you a better work life balance.

A good work life balance is also promoted through their flexible working schedule. It is possible to work 0.8 FTE, giving you more time for other projects, family time, etc. It is also possible to work a four day week (40 hours over 4 days) meaning you can benefit from more days off while not missing out on pay or experience.


  • Act as single point of contact for assigned trials and studies
  • Ensure adherence to SOPs
  • Perform study start up, regulatory and maintenance activities
  • Negotiate site contracts and budgets
  • Maintain internal systems and databases
  • Work with EC submissions


  • Master''s degree in life sciences or relevant combination of experience and education
  • 2 years minimum experience in clinical research with a focus on study start up
  • Professional fluency in Dutch and English, French language skills is also a plus
  • EC Submission experience
  • Open to CRAs with 2-3 years experience who are looking for a change


  • Market-leading salary and benefits package
  • Flexible work schedule
  • Sponsor dedicated
  • Tailored approach to your career development offering unparalleled opportunities for career progression

If this job appeals to you please apply here or send your CV to me, Eoin Meikle, on the NonStop Consulting website or on my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.

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, Romania, Luxembourg, US 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.

Posted: 24/05/2022 | NPJ Ref: 306530
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