Day-to-day delivery of Global Regulatory Affairs support services.
Manage clinical trial applications to authorities, ethics committees and regulators.
Develop stakeholder tools and regulatory risk assessments; represent the unit.
Ensure high quality, timely service in line with regulatory standards.

🎯 Requirements

Undergraduate degree with 4–6 years in Clinical Research/Regulatory Affairs.
Knowledge of LATAM clinical trial regulations.
Fluency in English and Spanish (written and verbal).

🎁 Benefits

Home-based role.
Accommodations for applicants with disabilities upon request.

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