Manage daily 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 with sponsors, researchers and regulatory authorities.
Ensure high quality, timely service per regulatory standards.
May coach peers and contribute to staff performance reviews.

🎯 Requirements

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

🎁 Benefits

Remote/home-based work arrangement.
Accommodations for applicants with disabilities available upon request.

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