Clinical Research Associate

Upsilon Global; Santo André; Presencial; BRL 78 000 - 134 000; Tempo integral

Resumo da oferta

A Upsilon Global está abrindo oportunidade para um(a) Clinical Research Associate freelancers no Brasil, sob contrato, para apoiar um estudo de Doença Infecciosa. Procuramos profissionais com experiência em CRA, monitoramento de sites e papel ativo em ensaios clínicos internacionais.

É desejável fluência em Português e Inglês, disponibilidade para atuação freelance e residência no Brasil. A vaga oferece experiência em ambiente internacional com entrega de alta qualidade, em regime de contrato.

Qualificações

• Experiência prévia como CRA em ensaios clínicos.
• Forte compreensão de monitoramento de sites e atividades de ensaios.
• Conhecimento de ICH-GCP e processos de pesquisa clínica.

Responsabilidades

• Monitorar sites e atividades de ensaios clínicos.
• Aplicar normas ICH-GCP e padrões de qualidade.
• Comunicar-progressos e possíveis questões à CRO internacional.

Conhecimentos

CRA experience

Site monitoring

ICH-GCP knowledge

Portuguese & English

Based in Brazil

Freelance/contract availability

Infectious Disease experience

Descrição da oferta de emprego

Clinical Research Associate Upsilon Global santo andré, estado de são paulo, br

Descrição da vaga

Join a growing international CRO and take the next step in your Clinical Research career.

We are looking for a Freelance Clinical Research Associate (CRA) in Brazil to support an exciting Infectious Disease clinical trial.

Our client is an international CRO supporting clinical research programs across a range of therapeutic areas, with a strong focus on scientific expertise, collaboration, and high-quality clinical delivery.

This is a great opportunity for a CRA looking to gain further experience within an international environment, and we are particularly interested in speaking with professionals who may be considering their first freelance/contract opportunity.

Key Requirements:

• Previous experience working as a CRA within clinical trials
• Experience with site monitoring and clinical trial activities
• Strong understanding of ICH-GCP and clinical research processes
• Fluent in Portuguese and English
• Ideally based in Brazil
• Available to work on a freelance/contract basis
• Previous Infectious Disease experience would be advantageous

You do not need to have previous freelance experience — if you have a solid foundation as a CRA and are looking to make the move into contracting, we would be very interested in speaking with you.