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Descripción de la vacante
Worldwide Clinical Trials is seeking a Specialist, Site Contracts to draft, negotiate, and finalize site agreements and amendments. You will review budgets, coordinate translations, and escalate risks with internal teams to ensure compliant, timely contract execution. Strong English, contract management software proficiency, and ability to manage multiple sites are essential. This role offers remote work with international scope.
Formación
Bachelor’s degree or equivalent in business, finance, science, or related field.
1–3 years in CRO/pharma/clinical research with investigator/site contracts or related legal field.
Excellent English written and verbal communication skills.
Responsabilidades
Prepare country contract templates and site agreements.
Negotiate contract language and budgets with sites to finalization/execution.
Coordinate with legal, regulatory, and study teams for submission and sign-off.
Maintain tracking tools for contract lifecycle and timelines.
Facilitate contract signatures and distribution to sites and sponsor.
Conocimientos
Contract negotiation
Regulatory compliance
Communication
Collaboration
Technical proficiency
Problem solving
Time management
Educación
Bachelor’s degree or equivalent in business/admin, finance, science, or related field
Herramientas
Contract management software
Microsoft Word
Excel
Descripción del empleo
Worldwide Clinical Trials is seeking a Specialist, Site Contracts to draft, negotiate, and finalize site agreements and amendments. You will review budgets, coordinate translations, and escalate risks with internal teams to ensure compliant, timely contract execution. Strong English, contract management software proficiency, and ability to manage multiple sites are essential. This role offers remote work with international scope.
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