RPS has now strongly developed its activities across Europe and due to our constant growth we are currently looking for Clinical Trials Assitant - Regulattory Affairs Assocaite to be resposible for:
- Regulattory submissions to Ethic Comitees and Regulatory Agencies
- Contract Management
- Investigators Payment
If you want to join an international job environment in a dynamic company which is in expansion this is the opportunity you are looking for.
Requirements:
- Studies in Administration or Health Sciences
- English and Spanish
- Minimum 3 years of experience as CTA in Regulatory Department
We offer:
- Permanent contract
- Social Benefits: Medical Assurance, 27 vacation days, english lessons
- Flexible working hours
