Clinical Research Associate

Upsilon Global; Hortolândia; Presencial; BRL 80 000 - 130 000; Tempo integral

Resumo da oferta

Upsilon Global is seeking a Freelance Clinical Research Associate (CRA) in Brazil to support an infectious disease trial within an international CRO framework. This is a contract/freelance opportunity ideal for someone expanding into contracting.

You will perform site monitoring, ensure ICH-GCP compliance, and collaborate with study teams. Portuguese and English fluency preferred; prior CRA experience in clinical trials with infectious disease exposure is advantageous, and Brazilian-based

Qualificações

• Previous experience as a CRA in 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.
• Infectious disease experience would be advantageous.

Responsabilidades

• Monitor clinical trial sites and activities according to study protocol and ICH-GCP guidelines.
• Collaborate with study teams to ensure data integrity and regulatory compliance.

Conhecimentos

CRA experience

Site monitoring

ICH-GCP

Portuguese/English bilingual

Based in Brazil

Freelance/Contract

Infectious Disease experience

Descrição da oferta de emprego

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.

If you're looking to build your CRA experience while supporting an exciting international clinical trial,