Posted 18 hours ago
Clinical Research Intern (Regulatory)
CPQuali (QIMA)Estagiário em Pesquisa Clínica (Regulátorio)
Perks & benefits
TransportationAnnual LeaveHealth Insurance
Requirements
Studying Biomedicine, Pharmacy, or related fields, Intermediate to advanced English, Microsoft Office proficiency, Strong organizational skills
Skills
Clinical ResearchRegulatory Affairs
About the role
Responsibilities
- Assist the team in detailed analysis and submission of the entire documentary cycle to the CEP/CONEP system via Plataforma Brasil
- Help prepare initial packages and amendments through to the reporting of serious adverse events (SAEs), notifications, and progress/closure reports
- Support monitors and the team during initiation, monitoring, and study closure visits, ensuring the integrity and rigorous organization of Investigator Site Files (ISF)
Requirements
- Currently studying Biomedicine, Pharmacy, or related fields (from 2nd semester onwards)
- Intermediate to advanced English
- Proficiency in Microsoft Office (Word, Excel, PowerPoint)
- Strong organization and attention to detail
- Proactivity and adaptability
Benefits
- Monthly stipend (Bolsa)
- Transportation voucher
- Birthday day off
- SESC partnership
About the Company
CPQuali, now a QIMA company, is a clinical research center with national operations and a complete structure for conducting Phase II, III, and IV studies.
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CPQuali (QIMA) · Sao Paulo
