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Contract Specialist II, Site Agreement / Contract & Budget Specialist - FSP Team - Italy

Remote, USA Full-time Posted 2026-06-25

The Site Budget & Contracts Specialist is responsible for drafting, negotiating, and managing site agreements and related clinical trial contracts for Sponsor-led studies. The role ensures timely execution of agreements, compliance with SOPs and ICH-GCP principles, and close collaboration with cross‑functional clinical study teams.

Key Responsibilities

  • Draft, review, negotiate, and process site agreements, templates, and related clinical trial contracts in accordance with Fortrea policies and Sponsor requirements.
  • Manage the full contract lifecycle, including tracking, approvals, execution, filing, and status updates using SAMS or equivalent systems.
  • Independently manage assigned studies while ensuring strict adherence to SOPs, quality standards, and regulatory requirements.
  • Identify contractual risks or operational delays early and escalate issues proactively to ensure timely resolution.
  • Coordinate with clinical study teams, project management, business development, and budget teams to align contract timelines and expectations.
  • Provide regular and accurate contract status updates to management and internal stakeholders.
  • Contribute to departmental objectives, process improvements, and support junior colleagues as required.

Experience & Qualifications

  • 3 - 5 years’ experience in clinical contracts, site agreements, or contract administration within a CRO or pharmaceutical environment.
  • Demonstrated experience in contract drafting, negotiation, and lifecycle management.
  • Solid knowledge of ICH-GCP, SOP-driven environments, and clinical trial regulations.
  • Bachelor’s degree preferred (Law, Business, or Life Sciences); law degree (EU) is an advantage.
  • Strong organizational skills with the ability to manage multiple studies simultaneously.

This is an excellent opportunity to contribute to global clinical studies while further developing your clinical contracts expertise within a dynamic CRO environment.

Learn more about our EEO & Accommodations request here.

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