Site Budget & Contract Specialist - Sponsor-dedicated

Fortrea; Paris; Hybride; EUR 65 000 - 90 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Remote/hybrid options

Growth opportunities

Cutting-edge projects

Résumé du poste

Fortrea seeks a Site Budget & Contract Specialist to negotiate and manage site agreements, confidentiality agreements, and letters of indemnification supporting our clinical trials in a fast-paced environment.

Join our FSPx team and collaborate with sponsor teams to advance development of innovative medications, ensuring compliance and timely execution of contracts across global studies.

Qualifications

• Bachelor's degree preferred; law degree highly desirable (UK/EU).
• Fortrea may consider equivalent relevant experience in lieu of education.
• 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 contract tracking systems.

Responsabilités

• 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 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.

Connaissances

Contract negotiation

Clinical research

Regulatory compliance

ICH GCP familiarity

Negotiation

Communication

Organizational skills

Independent work

Microsoft Office

Contract tracking systems

Formation

Bachelor’s degree

UK/EU law degree desirable

Equivalent relevant experience considered

Outils

Microsoft Office

Contract tracking systems

Description du poste

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

• 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 mandate 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

• 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.