Clinical Contract Associate

Step into an exciting opportunity at Excelya, a leading Contract Research Organization (CRO) dedicated to advancing healthcare through innovative clinical research. Join our dynamic team as a Clinical Contract Associate and contribute to managing clinical contracts that enable groundbreaking studies worldwide.

The role focuses on preparing, reviewing, negotiating, and tracking Clinical Trial Agreements (CTAs) and related documents in alignment with Legal guidance and internal company policies. The Clinical Contract Associate acts as a key operational interface between Clinical Operations, Legal, Procurement, Finance, Compliance, service providers, and clinical sites.

Key Responsibilities:

• Draft, review, negotiate, execute, and archive clinical trial and clinical project-related contracts in accordance with approved templates and legal guidance.
• Support R&D Legal in the review of complex agreements or MSAs when requested.
• Serve as the primary point of contact for contractual matters with clinical sites and service providers.
• Monitor contract execution, amendments, extensions, renewals, and close‑out activities.
• Track and control the contract signature and approval process to ensure compliance with company requirements.
• Manage Power of Attorney (POA) documentation granted to service providers, when applicable.
• Identify and resolve low‑risk contract issues independently, escalating higher‑risk matters to R&D Legal.

• Work closely with Clinical Operations teams, Legal, Procurement, Finance, Compliance, and external partners to ensure appropriate contractual coverage for all clinical trials.
• Ensure adherence to legal and compliance guidelines regarding acceptable changes to standard terms and conditions.
• Communicate contract status, risks, and timelines clearly to internal stakeholders.
• Support the RFP and vendor selection process in collaboration with Clinical Research Management and Procurement.

• Stay informed on evolving clinical trial contracting practices and country‑specific contractual requirements.
• Support the continuous improvement of standard templates, workflows, and contract management processes.
• Contribute to training initiatives related to clinical contract management.
• Proactively escalate contract delays or issues to R&D leadership when required.
• Provide backup and operational support to other Clinical Contract Specialists when needed.

Qualifications and Skills:

• Law degree or equivalent qualification, or experience in clinical trial contract review within a pharmaceutical or CRO environment.
• Strong understanding of standard clinical trial agreement clauses and country‑specific variations.
• Experience negotiating with clinical sites and service providers across international regions.
• Excellent communication and interpersonal skills, with fluency in English.
• Attention to detail and commitment to compliance with regulatory and company standards.

Why Join Us? At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare. Here's what makes us unique We are a young, ambitious health company representing 900 Excelyates, driven to become Europe's leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey. Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.