Regulatory Affairs SpecialistLocation: Brasília, Distrito FederalCompany: Upsilon GlobalUpsilon 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
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