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Regulatory Clinical Associate - Close to Start-Ups - Leuven

Employer
NonStop Consulting
Location
Leuven
Salary
Negotiable
Closing date
Apr 14, 2018

View more

Sector
Pharmaceutical, Regulatory Affairs
Contract Type
Employee
Hours
Full Time
Organization Type
Corporate

Job Details

A CRO is looking for a Regulatory Clinical Associate because they started new big projects with pharmaceutical companies. They work mainly with innovative start-ups in the pharmaceutical and medical device field which gives you the chance to be closer to more interesting and rare products. The communication with start-ups will also be faster and more efficient.

You will work closely with the owner of the company who is really passionate about her business. You will get more involved in all the projects and have strong support from the owner. Accordingly, you will keep developing your skills.

Profile:

  • Master Degree in life sciences or equivalent by experience
  • Experience in Regulatory Affairs for clinical studies for the pharmaceutical or medical device industry
  • Ideally previous experience as CTA or CRA
  • Fluent level in Dutch, French and English

Your responsibility is to consult clients on the regulatory requirements during clinical studies and prepare the necessary documents. Every project could have a different focus so you will get some variety in tasks.

If you like the combination of clinical and regulatory, please send me, Annelies De Baere, your most recent CV in Word format to a.baere@nonstop-recruitment.com or call me on +32 2 403 49 80. If you are not interested but could recommend someone in your network, do not hesitate to send me their contact details.

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.

What I offer: As a specialist Headhunter within Regulatory Affairs for the pharmaceutical industry in Belgium I have a strong market knowledge and good relationships with companies. Therefore I will not just find you suitable roles but also offer you accurate, honest advice and provide you with inside information of the team/company culture.

Key words: Regulatory Affairs/Associate/Officer/Specialist/Benelux/Belux/Belgium/CTA/CRA/Clinical Trials/Clinische Studies/Clinical Research /Pharmaceutical/Pharma/Belgique/Belgie/CRO /French/Dutch/RA

Company

Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries. 

Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery.  Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.

The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors. 

Company info
Website

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