Clinical Trial Contract Specialist

Overview

As a Site Contracts Specialist you’ll own the contract lifecycle for clinical studies, from drafting to finalization, within Medpace’s Site Contracts Team in Italy. You will negotiate within approved templates, assess risks, and coordinate with internal teams to align site startup activities with contractual timelines. You’ll stay current on local regulatory requirements affecting contracts and support cross-functional touchpoints to enable study start-up. This role offers growth in a globally respected CRO with a patient-focused mission and impact on trial execution.Responsibilities

• Draft, review, negotiate, and finalize clinical study agreements and related legal documents
• Negotiate within client-approved templates and parameters
• Identify legal, financial, and operational risks and elevate when needed
• Provide recommendations and alternative resolutions during negotiations
• Coordinate with internal functions to align site startup activities with contractual timelines
• Maintain up-to-date knowledge of applicable local regulations affecting contracts

Qualifications

• Bachelor degree
• At least 1 year of relevant work experience
• Strong Italian and English written and spoken communication skills
• Strong attention to detail
• Prior contract negotiation experience preferred but not required

Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

#J-18808-Ljbffr