Job Reference: 1412-85
Job Duration:
Start date: a.s.a.p
Description:
My client is a leading pharmaceutical companybased in the centre of Paris and they specialise in the development of human and veterinary medicine. Within this role you will gain exposure to extensive clinical development programs in oncology and in inflammatory and neurodegenerative diseases, including 20 phase 1 and 2 studies on going in France and 10 Phase 3 trials in over twenty countries. As part of the expansion of its business volume, the company is seeking a Regulatory Submission Manager to join their team and you will ideally have the following experience:
Responsibilities:
*You will have primary responsibility for the coordination , preparation and submission of regulatory dossiers for clinical trials in Germany and Austria.
*Review the documents in the file and confirm completeness
*Analyze and implement new regulatory needs
*Respond to regulatory matters agencies and ethics committees in Germany and AustriaExperience:
* Significant experience in the implementation of clinical trials and regulatory submissions
* Thorough knowledge of clinical development of regulations
* German and Fluent English language skills are essential
For further details about this role or other opportunities within Regulatory Affairs please contact Tim Barratt on +44 (0) 1727 817 626 or email a copyof your CV to tbarratt@keypeople.co.uk
Key People is a recruitment consultancy with a reputation for providing good value that's been built up over 20 years. Clients come to us for three main reasons:
> We achieve results faster
> Our candidates really are a cut above
> We add greater value
We think it's because we're a private company driven by clients, not by shareholders.
For our candidates, we have developed relationships with thousands of clients nationwide, throughout Europe and also many around the globe, who choose to recruit through Key People, so you'll have a wide choice of opportunities to further your career. And, as we work for 75% of FTSE 100 companies, you'll get the chance to work for some prestigious, blue-chip organisations.
Industry: Pharmaceuticals
Salary: €45000 - €60000 per annum + benefits
Salary Benefits: benefits
Vacancy Type: Permanent
Job Skills: submissions manager, regulatoryaffairs, clinical, CTAs, IMPDs, ethics submissions
Contact Name: Tim Barratt
Website: -
Direct Application URL: -