Site Budget & Contract Specialist

Posted Yesterday
Be an Early Applicant
2 Locations
In-Office
Mid level
Biotech
The Role
Negotiate, prepare, and manage site agreements, confidentiality agreements, and indemnification letters for clinical trials; ensure regulatory and SOP compliance; track contract status; collaborate with study teams, legal, and project management; maintain contract files; escalate issues and support process improvements.
Summary Generated by Built In

Join Our Team and Shape the Future of Clinical Research!

At Fortrea, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist, you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency.

In this role, you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications.

Key Responsibilities:

In this role, you will:

  • Prepare, negotiate, and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials.

  • Ensure compliance with SOPs, regulatory guidelines, and contractual obligations.

  • Track, update, and maintain contract status in relevant systems, ensuring transparency and timely execution.

  • Identify and escalate contractual issues to management as needed.

  • Support the internal review, revision, and approval process of contracts before forwarding them to external parties.

  • Collaborate with clinical study teams, legal, and project management to ensure seamless contract execution.

  • Maintain electronic and paper contract files, ensuring accuracy and accessibility.

  • Assist in the continuous improvement of departmental processes and procedures.

  • Provide regular status updates to management and study teams.

Required Qualifications:

To succeed in this role, you should have:

  • Bachelor’s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable (UK/EU).

  • Fortrea may consider equivalent relevant experience in lieu of educational requirements.

  • 2–4 years of experience in contract negotiation, clinical research, or a related field.

  • Strong understanding of ICH GCP guidelines and clinical research processes.

  • Excellent negotiation, communication, and organizational skills.

  • Ability to work independently and manage multiple priorities in a fast-paced environment.

  • Proficiency in Microsoft Office and contract tracking systems.

What We Offer:

  • Competitive salary and performance-based incentives.

  • Flexible work arrangements (remote/hybrid options).

  • Professional growth opportunities in a collaborative and innovative environment.

  • The opportunity to work on cutting-edge clinical research projects.

Ready to Make an Impact?

Take the next step in your career and join us in driving innovation in clinical research.

Apply today! Applications are reviewed on a rolling basis—don’t miss this opportunity!

#LI-Remote #LI-Hybrid

Learn more about our EEO & Accommodations request here.

Skills Required

  • 2-4 years of experience in contract negotiation, clinical research, or related field
  • Strong understanding of ICH GCP guidelines and clinical research processes
  • Excellent negotiation, communication, and organizational skills
  • Ability to work independently and manage multiple priorities in a fast-paced environment
  • Proficiency in Microsoft Office and contract tracking systems
  • Bachelor's degree (LLB, JD, BA, or BS)
  • University-level law degree (highly desirable, UK/EU)
  • Equivalent relevant experience may be considered in lieu of education
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The Company
HQ: Research Triangle Park, NC
10,811 Employees

What We Do

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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