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Ctry Approval Assoc FSP @ Thermo Fisher

Remote, ArgentinaRemoteFull-time
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About this role

Embrace the opportunity to become a Country Approval Associate and play a key role in preparing and coordinating regulatory submissions for clinical trials. Collaborate with cross-functional teams, ensure compliance with local and global guidelines, and help drive successful site activations. Ideal for detail-oriented professionals eager to launch their careers in clinical research.. Category: Clinical Research

Skills

regulatory submissionsmedical terminologyethical committee submissionsclinical trial coordinationregulatory compliancepatient information sheet developmentinformed consent form developmentgrant budget negotiationdatabase entrysop compliancecomputer skillsenglish language proficiencyattention to detailplanning skills

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