Regulatory Affairs Specialist
Location: Brasília, Distrito Federal
Company: Upsilon Global
Upsilon Global has partnered with a CRO to support an ongoing Cardiovascular Study in Brazil. We are seeking a Regulatory Affairs Specialist to join the team and support this project.
Responsibilities:
* Manage regulatory submissions and documentation for clinical trials in Brazil.
* Coordinate with regulatory authorities and internal teams to ensure compliance.
* Keep updated with current regulations and guidelines affecting clinical research.
Qualifications:
* Experience in regulatory affairs within the healthcare or pharmaceutical industry.
* Knowledge of Brazilian regulatory requirements for clinical studies.
* Excellent communication and organizational skills.
Application deadline: 16/04/2025
#J-18808-Ljbffr