We are in the process of recruiting a bi-lingual (English) Regulatory Affairs Associate to work from our office in Sao Paulo. As a Regulatory Affairs Associate you will coordinate the regulatory workflow to obtain clinical trial approvals from regulatory authorities, provide regulatory consultancy to the team, and interface with the project team, the sponsor and regulatory authorities on strategic regulatory and technical matters for Brazil and other Latin American countries.
To be considered for this role, you must have experience working in a CRO in a regulatory role. Fluency in English is required as well as a university degree in health science or pharmacy.
Please submit English CV for consideration.
- CRO work experience in Regulatory submissions
- Education in health sciences or pharmacy
- Solid experience with computer systems
- Fluency in written and spoken English