Clinical Regulatory Affairs Manager - Medical Devices Projects
A medical devices service provider is looking for a Regulatory Affairs Manager to work on different projects for their medical devices clients. It means you will have more variety in the activities and will be able to build your network with professionals in the medical devices industry because you will work as an intermediary between all the involved stakeholders.
You will be responsible for the regulatory aspects within clinical research studies which means you are working closer to patients and are more aware of new developments on the market.
This is a permanent contract within the CRO where you will work in-house and do not have to commute to the offices of the clients, so you do not have to worry about being stuck in traffic or to get frustrated about the locations of the clients.
- Master Degree in Life Sciences, or equivalent by experience
- Some years experience in Regulatory Affairs for the Medical Devices or Pharmaceutical industry
- Experience in Clinical Research setting
- Strong organisation skills
- Fluent level of English, Dutch or French is a plus
If this job appeals to you please apply here or send your CV to me, Annelies De Baere, on the NonStop Recruitment website or 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 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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