
Site Contract Specialist
Posted Sep 4

Posted Sep 4
This is a fully remote position, open to applicants in Spain.
• Establish initial site contact and follow up as needed to finalize study confidentiality agreements (CDAs) and clinical trial agreements (CTAs) drafts.
• Manage contract language in accordance with approved sponsor guidelines and collaborate with legal counsel for contract revisions and negotiations.
• Oversee the completion and execution of CDAs and CTAs.
• Participate in both internal and external project team meetings, providing updates on the progress of CDAs and CTAs.
• Organize contract files and maintain both internal and external CDA and CTA tracking sheets.
• Update the status of CTAs in the internal study start-up module for the studies assigned.
• Support contract preparation, review, revision, execution, and filing processes.
• Inform relevant parties about critical terms, including expiration dates, renewal terms, and compliance requirements.
• Assist in the preparation, review, negotiation, execution, and filing of CDAs.
• Maintain records and archives for CDAs.
• Process paperwork for new consultants and keep their files organized.
• Paralegal certification or an Associate's degree.
• A minimum of two years of experience in a professional administrative or business role.
• Proficiency in both spoken and written Italian and English.
• Applications must be submitted in English.
• Structured mentoring program.
• Leadership development courses.
• Dedicated training department.
• Ongoing education support.
• Hybrid work opportunities.
• CTI Cares community and charitable engagement program.
• Support for work-life balance.
IQVIA
Thermo Fisher Scientific
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