Associado de Pesquisa Clínica em Sao Paulo

As a Clinical Research Associate, you'll serve as the primary liaison between Novo Nordisk and clinical trial sites, taking ownership of study execution while building meaningful relationships with investigators and site staff

You'll be at the heart of clinical trials that could change millions of lives

The role involves conducting remote and on-site visits including selection, initiation, interim monitoring, and study closure for oncology clinical trials

This role offers the opportunity to work at the forefront of oncology science to transform cancer treatment practices

This role serves as the primary contact point between the Sponsor and Investigational Site to ensure inspection readiness through strict compliance with GCP and company SOPs

This role offers the opportunity to work at the forefront of oncology science, contributing to studies that can transform medical practice

The role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets

The role supports the Regional Clinical Study Manager in delivering regional studies while ensuring execution meets quality standards, timelines, and budget

This role serves as the primary contact point between the Sponsor and Investigational Sites to ensure inspection readiness and compliance

This role serves as the primary contact point between the Sponsor and Investigational Sites to ensure inspection readiness and compliance

This role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness

The role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets

The role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets

The role supports the Regional Clinical Study Manager in executing regional study delivery while ensuring adherence to quality standards, timelines, and budgets

This role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring adherence to quality standards, timelines, and budgets

The role supports the Regional Clinical Study Manager in delivering regional study components while ensuring execution meets quality standards, timelines, and budget

The role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring execution meets quality standards, timelines, and budget

This role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness through strict compliance with protocols and regulations

The role supports the Regional Clinical Study Manager in delivering regional clinical studies while ensuring execution meets quality standards, timelines, and budget

This role serves as the primary contact point between the Sponsor and Investigational Site to ensure inspection readiness through strict compliance with protocols and regulations

The role involves proactively solving study-related clinical site issues to ensure successful protocol level execution across start-up, execution, and close-out phases

ICON plc is seeking a Graduate Pharmacovigilance Associate to support the safety monitoring and reporting of pharmaceutical products

ICON plc is a world-leading healthcare intelligence organization seeking a Clinical Research Associate to join their diverse team in São Paulo

The role involves leading the identification, selection, activation, and maintenance of clinical sites for complex oncology trials across the LATAM region

The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements