Senior Site Contracts Specialist, Spain — Clinical Trials

Worldwide Clinical Trials

Madrid

On-site

EUR 45,000 - 65,000

Full time

2 days ago
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Job summary

Worldwide Clinical Trials in Madrid is seeking a Senior Site Contracts Specialist to lead negotiation and finalization of clinical trial site contracts and budgets. You will act as a SME on CTA processes at country and site level, coordinating with sponsors, sites and internal teams.

The role requires deep knowledge of ICH-GCP, regulatory requirements, and strong cross‑functional collaboration. Join a global CRO that values quality, patient outcomes, and career growth.

Qualifications

  • Experience negotiating complex site contracts and budgets.
  • Strong understanding of ICH-GCP and local regulatory requirements.
  • Ability to explain contract terms clearly to diverse stakeholders.
  • Familiarity with vendor management and oncology/clinical trials industry.

Responsibilities

  • Act as SME on Clinical Trial Agreement processes at country and site level.
  • Preparation, negotiation and finalization of site contracts and budgets.
  • Manage the Investigator Budget and liaison for contract communications.
  • Resolve negotiation issues, escalate risks, and improve SOPs.
  • Collaborate with Worldwide stakeholders and external stakeholders (sites, investigators, etc.).
  • Review and finalize CTAs and related documents for completeness and accuracy.

Skills

Contract negotiation
Regulatory knowledge
Cross-functional collaboration
Leadership
Clear communication

Education

Bachelor's Degree or equivalent in business administration, finance, law, science or related field

Tools

MS Word
Excel
Outlook

Job description

Worldwide Clinical Trials in Madrid is seeking a Senior Site Contracts Specialist to lead negotiation and finalization of clinical trial site contracts and budgets. You will act as a SME on CTA processes at country and site level, coordinating with sponsors, sites and internal teams.

The role requires deep knowledge of ICH-GCP, regulatory requirements, and strong cross‑functional collaboration. Join a global CRO that values quality, patient outcomes, and career growth.

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