RPS has now strongly developed its activities across Europe and due to our constant growth we are currently looking for a Start-up Specialist to be responsible for regulatory submissions to Ethic Comities and Regulatory Agencies in local and international clinical trial studies.
Requirements:
- Minimum 3 years of experience in regulatory submissions for local and international studies.
- Experience in Clinical Trial Applications
- Studies in Administration or Health Sciences
- English and Spanish
We offer:
- Permanent contract
- Social benefits: medical assurance, day-care subsidy, English lessons, 27 vacations days, flexible working hours and reduced hours every Friday.
