Regulatory Submissions Manager - Belgium - multinational CRO

작업 내용

Are you currently working in aCRO and looking to move your career forward to Regulatory Affairs? This is a chance to do so. We are in search of a Regulatory Submissions Manager based in Leuven, Belgium to support this quality multinational CRO’s daily operations. The company is focused on hiring the most talented people and are offering a lot of support in promotion As a Regulatory Submissions Manager you will perform quality checks on submission documents and site essential documents and be reviewing the consent forms.

What do you need to join?

• At least 4 years of experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
• Knowledge and experience of Clinical Trial Applications within Europe;
• Strong oral and written communication skills;
• Team oriented approach and strong leadership skills; and
• Fluency in English.
  

What do we offer?

• Competitive salary;
• An attractive set of benefits;
• Great company atmosphere;
• Many opportunities to grow and learn.
  

Sounds interesting? If you want to know more, please apply here or the NonStop website. You can also contact me, Aneta Krawczynska, on my phone number +41 435 080 817 ext. 3624 or A.Krawczynska@nonstop-recruitment.com. I would not mind being reached out directly on LinkedIn either. If the offer does not feel suitable for you but you know someone who might be interested, you are welcome to help them and forward their profile.

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 EU countries. Please visit our website for a full list of the niche markets we cover.