Site Contract Specialist I
Share role
The recipient sees their own assessment. Your profile and score are not shared.
About the role
Remote, home-based role in Colombia supporting clinical research study start-up activities. Responsibilities include reviewing and negotiating site budgets, clinical trial agreements and investigator grants; preparing and tracking contracts; coordinating signatures; maintaining trial documentation; and liaising with legal, translation and project teams. A college/university degree or equivalent education, training and experience, fluency in Spanish and English, and previous study startup operations experience are required.
Key requirements
- • College/University degree or an equivalent combination of education, training & experience
- • Required skills: Study startup operations, Clinical trial agreement review and negotiation, Site budget review and negotiation, Investigator grant negotiation, Contract preparation and execution, Clinical Trial Management System (CTMS), Trial Master File documentation, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Planning, Communication, Collaboration
- • Required languages: Spanish, English
Opportunity details
- • Workplace: Remote
- • Posted: Sep 8, 2026
- • Original advert language: English
Full vacancy
HealthRoleIQ regularly verifies this opportunity against the employer’s posting and highlights the details relevant to your match.
See original vacancy ↗Employer’s role description
Job title: Site Contract Specialist I
Location: Bogotá, Bogota, Colombia
Employment type: Full-time
Workplace type: Remote