Experteer Overview

Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud.

In this role, you will manage the end-to-end lifecycle of clinical trial contracts, from drafting to finalization, ensuring alignment with client templates and regulatory requirements. You will collaborate with cross-functional teams to support site startup activities and mitigate legal and budgetary risks. The position sits within the Site Contracts Team in Spain, contributing to Medpace’s mission to accelerate general development of medical therapeutics.

You will work in a fast-paced, learning-oriented environment that values cross-functional collaboration and continuous improvement. This is a growth-focused role with meaningful impact on trial timelines and compliance.

Compensaciones / Beneficios

- Draft, review, negotiate, and finalize agreements and related legal documents for clinical studies
- Negotiate within client-approved contract and budget templates and parameters
- Identify and assess legal, financial,



and operational risks; escalate as needed
- Provide recommendations and alternative resolutions during negotiations
- Coordinate with internal departments to ensure startup activities align with contractual processes and timelines
- Stay updated on local regulations impacting clinical trial contracts

Responsabilidades

- Bachelor's degree; preferably in Law or Sciences
- At least 1 year of relevant work experience
- xugodme Prior contract negotiation experience preferred but not required
- Strong attention to detail
- Strong Spanish and English written and spoken communication skills

Requisitos principales

- competitive compensation
- comprehensive health, wellness, retirement, and PTO
- office-based with occasional WFH after training
- onboarding and ongoing training programs
- career development opportunities
- employee-focused culture and social events

📌 Clinical Trial Contract Specialist (Madrid)
🏢 Medpace
📍 Madrid