- Want to work for a world leading Biopharmaceutical Company in Switzerland? - Is Clinical Trials Regulatory Affairs your area of expertise? - Want a diverse and challenging role which will cover managing CROs, leading cross functional activities and other tasks beyond just CTAs?
Specialist/Senior Specialist, Regulatory Affairs (Clinical Trials group) Location: Neuchâtel region of Switzerland, bordering France Salary: Between 100-120,000 Swiss Francs per annum Possibility of a relocation package for the right candidate
Job reference: J23650
Our client, a leading innovative biopharmaceutical company have recently released to us a Specialist or Senior Specialist role within their Regulatory Affairs Clinical Trials Group. The right individual will be managing their CTAs to Health Authorities across the EEA region
Job Description: - Prepare coordinate and submit CTAs across the EEA - Work and liaise closely with Regulatory Leads, Study Team members and CROs - Maintenance of CTAs during its life cycle - Tracking CTA activities and QC of CTA package - Propose process improvements and/or new processes for CTA outsourcing
Job Requirements: - Minimum of 6 years' experience within Clinical Trials Regulatory Affairs - Experience working at the Specialist level - Strong EU submission experience, National (Switzerland) is desirable - Good knowledge of EU Clinical Trial Directive
This is a great opportunity for work within a highly reputable biopharmaceutical company, if you are looking for you next contract position the please get in touch asap, call Adam on (0) .
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