- Would you like to work for a world leading Biopharmaceutical Company based in Switzerland? - Would you class yourself as a Clinical Trial and Regulatory Affairs expert? - Are you looking for a more challenging opportunity that will give you exposure to areas you may not have had yet?
Location: Neuchâtel region of Switzerland, bordering France Salary: Between 100-120,000 Swiss Francs per annum Relocation package available for candidates willing to relocate
I am now working with a leader within the Biopharmaceuitcal sector who is actively looking for a Senior Specialist to join there Regulatory Clinical Trial team. This candidate will be part of a cross-functional team working closely with Health Authorities and CRO"e;s to ensure the successful preparation and submission of clinical trial applications into the EEA markets.
Job Description: - Preparation, coordination and submission of CTAs across the EEA - Work closely with cross-cross functional teams, CRO"e;s and Health authorities - Manage the CTA"e;s throughout its full lifecycle - Tracking CTA activities and QC of CTA package - Propose process improvements and/or new processes for CTA outsourcing
Job Requirements: - At least 6 years' experience within Clinical Trials Regulatory Affairs - Strong EU affiliate experience - Strong EU submission experience, National (Switzerland) is desirable - Experience managing CRO"e;s desirable
This is an excellent opportunity for to work for a widely respected biopharmaceutical organisation so if you are looking for you next position then please get in touch asap, call Chris on (0) .
If you are not looking but know someone who is and would be suitable for this position then please forward their details to Chris Bart . We offer a referral scheme here at Regulatory Professionals, anyone you recommend to us and we then place you will receive €250 worth of voucher *terms and conditions apply