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

Fortrea

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profile Job Location:

milan - Italy

profile Monthly Salary: Not Disclosed
Posted on: 7 hours ago
Vacancies: 1 Vacancy

Job Summary

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 crossfunctional 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.
  • Bachelors 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.


Required Experience:

IC

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 crossfunc...
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