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Regulatory Submissions Manager
il y a 2 semaines
My Client who is a very successful, mid-size CRO are currently looking for a Regulatory Submission Manager to join their team in Leuven (Belgium). They are constantly growing, which allows for your personal growth as well as great opportunities to develop & grow your career. Along with that you will receive top quality training which has been voted one of the top training programs globally. As well as all of this you will have quarterly performance reviews allowing a lot of opportunity for promotions.
**Some of the responsibilities**:
Efficiently manage and successfully execute all aspects of global start-up
Perform quality checks on submission documents and site essential documents
Review pertinent regulations to develop proactive solutions to start-up issues and challenges
Prepare and approve informed consent forms
**Requirements**:
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
Fluency in English
NonStop Consulting 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
