Clinical Trial Site Agreement Specialist

hace 1 día


Madrid, Madrid, España Precision Medicine Group A tiempo completo
{"title": "Clinical Trial Site Agreement Specialist", "description": "Job Summary

We are seeking an accomplished Clinical Trial Site Agreement Specialist to join our European team. As a key member of our team, you will be responsible for reviewing, drafting, negotiating, and tracking a variety of legal agreements, including clinical study agreements, vendor contracts, and amendment agreements across various locations, mainly European ones.

Key Responsibilities
  • Review, draft, negotiate, and track clinical trial agreements and vendor contracts
  • Manage site contracting strategies for assigned projects
  • Negotiate site budgets and ensure deliverables are in alignment with defined study timelines
  • Work closely with the Clinical Operations study team to ensure successful project execution
Requirements
  • Strong relevant experience in drafting, reviewing, and negotiating clinical trial agreements and vendor contracts
  • Full responsibility for site contract management from setting up site contracting strategy to execution of contracts
  • Strong site budget negotiation experience
  • Experience within CRO, life science, biotech, or pharmaceutical industry
  • Excellent organizational and communication skills and attention to detail
What We Offer

Precision Medicine Group is a dynamic and innovative company that offers a unique opportunity to work with cutting-edge technology and a talented team. As a Clinical Trial Site Agreement Specialist, you will have the chance to develop your skills and expertise in a fast-paced environment and contribute to the success of our projects.

", "lang_code": "en-US"}

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