Site Budget & Contract Specialist

Remote Worker LTD.; United States; Hybrid; USD 90,000 - 130,000; Full time

Benefits offered by this job

Flexible remote/hybrid options

Competitive salary

Professional growth opportunities

Collaborative environment

Job summary

Fortrea is seeking a Site Budget & Contract Specialist to negotiate and manage site agreements and related documents for clinical trials. You will ensure compliance with SOPs and regulatory guidelines while tracking contract status across systems.

You will collaborate with clinical study teams, legal, and project management to drive timely contract execution and maintain accurate filing. Flexibility for remote/hybrid work is offered to support project needs.

Qualifications

• Bachelor’s degree or equivalent; law degree preferred (UK/EU).
• 2–4 years of contract negotiation or clinical research experience.
• Strong knowledge of ICH GCP guidelines and regulatory processes.
• Excellent negotiation, communication, and organizational skills.
• Ability to manage multiple priorities independently in a fast-paced environment.

Responsibilities

• Prepare, negotiate, and manage site agreements, confidentiality agreements, and indemnification letters for clinical trials.
• Ensure compliance with SOPs, regulatory guidelines, and contractual obligations.
• Track, update, and maintain contract status in relevant systems for transparency and timely execution.
• Elevate contractual issues to management when needed.
• Support internal review and approval processes before forwarding contracts to external parties.
• Collaborate with clinical study teams, legal, and project management for seamless contract execution.
• Maintain electronic and paper contract files with accuracy and accessibility.
• Assist in continuous improvement of departmental processes and procedures.
• Provide regular status updates to management and study teams.

Skills

Contract negotiation

Clinical research

Communication

Organizational skills

Independent work

Education

Bachelor or higher (LLB/JD/BA/BS) preferred

Equivalent relevant experience

Tools

Microsoft Office

Contract tracking systems

Job description

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 elevate 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.

Learn more about our EEO & Accommodations request here.