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Site Budget & Contract Specialist

Hybrid in Ireland·Full-time·Added 26 days ago (last checked 19 Oct)

Fortrea

1 open role

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Our summary

Work mode: Hybrid, Ireland
Contract: Full-time
Experience: 2+ years

Skills

Requirements

What we're looking for

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

Pay & benefits

What you'll get

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.

The role

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.

What you'll do

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.