Clinical Country & Site Associate (Clinical Trial Manager) - Sponsor dedicated

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Country & Site Associate (Clinical Trial Manager) - Sponsor dedicated based in Brazil.

This is a field- and site-focused clinical operations role at the heart of global clinical research execution, supporting sponsor-dedicated studies across multiple therapeutic areas.
You will ensure that clinical trial sites operate in full compliance with regulatory standards, ICH-GCP guidelines, and study protocols while maintaining high-quality data integrity.
The role combines on-site and remote monitoring responsibilities, requiring strong attention to detail and a proactive, problem-solving mindset.
You will work closely with investigators, site staff, and cross-functional clinical teams to support study start-up, execution, and close-out activities.
This position plays a critical role in safeguarding patient safety, ensuring data accuracy, and driving study performance across assigned sites.
It offers exposure to complex, global clinical trials within a fast-paced, highly regulated environment where precision and communication are essential.

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Country & Site Associate (Clinical Trial Manager) - Sponsor dedicated based in Brazil.

This is a field- and site-focused clinical operations role at the heart of global clinical research execution, supporting sponsor-dedicated studies across multiple therapeutic areas.
You will ensure that clinical trial sites operate in full compliance with regulatory standards, ICH-GCP guidelines, and study protocols while maintaining high-quality data integrity.
The role combines on-site and remote monitoring responsibilities, requiring strong attention to detail and a proactive, problem-solving mindset.
You will work closely with investigators, site staff, and cross-functional clinical teams to support study start-up, execution, and close-out activities.
This position plays a critical role in safeguarding patient safety, ensuring data accuracy, and driving study performance across assigned sites.
It offers exposure to complex, global clinical trials within a fast-paced, highly regulated environment where precision and communication are essential.

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

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