Regulatory Affairs Specialist – LATAM

Alimentiv

Responsible for the day-to-day activities in Global Regulatory Affairs including trial applications and compliance. Ensuring quality service delivery processes and potentially coaching peers.

Posted 7/13/2026full-timeRemote • 🇧🇷 BrazilMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Global Regulatory Affairs and Clinical Research, with a strong focus on LATAM clinical trial regulations. Capable of managing regulatory submissions and ensuring compliance with industry standards while providing high-quality service delivery.

Highest-signal resume keywords

Global Regulatory AffairsClinical Trial ManagementLATAM Clinical Trial RegulationsBilingual in English and SpanishStakeholder Engagement

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory Risk AssessmentClinical ResearchRegulatory SubmissionsService Delivery ProcessesCompliance Standards

Soft Skills

CoachingCollaborationCommunication

Industry Keywords

Competent AuthoritiesEthics CommitteesRegulatory AgenciesStakeholder Tools

About the role

Key responsibilities & impact

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services.
Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies.
Develop stakeholder tools, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities.
Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines.
May be required to coach peers and/or provide input for staff performance reviews.

Requirements

What you’ll need

Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
Fluency in English and Spanish (written and verbal) required.

Benefits

Comp & perks

Accommodations for job applicants with disabilities are available upon request.