Site Monitor II - FSP

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Site Monitor II – FSP based in Brazil.

This role is essential to ensuring the integrity, quality, and compliance of clinical trial data across assigned study sites within global research programs.
You will act as the primary point of contact for investigative sites, supporting them throughout the study lifecycle from initiation to close-out.
The position combines on-site and remote monitoring activities, with a strong focus on data quality, protocol adherence, and regulatory compliance under ICH-GCP standards.
You will build strong, collaborative relationships with site staff while proactively identifying and resolving operational and compliance issues.
A key part of the role is ensuring sites remain inspection-ready through continuous oversight, documentation review, and training support.
You will also contribute to study performance tracking, recruitment support, and issue escalation when required.
This is a dynamic field-based role where scientific rigor, communication, and attention to detail directly safeguard patient safety and study success.

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Site Monitor II – FSP based in Brazil.

This role is essential to ensuring the integrity, quality, and compliance of clinical trial data across assigned study sites within global research programs.
You will act as the primary point of contact for investigative sites, supporting them throughout the study lifecycle from initiation to close-out.
The position combines on-site and remote monitoring activities, with a strong focus on data quality, protocol adherence, and regulatory compliance under ICH-GCP standards.
You will build strong, collaborative relationships with site staff while proactively identifying and resolving operational and compliance issues.
A key part of the role is ensuring sites remain inspection-ready through continuous oversight, documentation review, and training support.
You will also contribute to study performance tracking, recruitment support, and issue escalation when required.
This is a dynamic field-based role where scientific rigor, communication, and attention to detail directly safeguard patient safety and study success.

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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