Senior Site Contracts Specialist – Global Trials

Worldwide Clinical Trials; United Kingdom; On-site; GBP 42,000 - 60,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Site Contract professional in the United Kingdom to draft, negotiate, and finalize site contracts and investigator agreements in alignment with budgets and study timelines.

You will review study budgets, liaise with Worldwide Legal and regulatory teams, and support cross-country approval and execution processes. Strong English and MS Word/Excel/Outlook proficiency are essential.

Qualifications

• Draft, review and negotiate country site contracts and investigator agreements.
• Review study budgets and contract costs to support negotiations and finalization.
• Understand international and local regulatory requirements for clinical trials (FDA/EMA/ICH-GCP).
• Communicate clearly with internal stakeholders and clinical sites to resolve issues.

Responsibilities

• Prepare country contract templates and related documents.
• Draft and send Site Agreements to sites to begin negotiations.
• Negotiate contract language and budgets with sites to finalization and execution.
• Review budgets and costs related to contract negotiation.
• Provide drafts to regulatory teams when needed; liaise with legal, data privacy, study teams, sponsors, and sites.

Skills

Contract negotiation

Regulatory knowledge

Communication skills

Analytical skills

Risk management

Education

Bachelor's Degree or equivalent in business administration, finance, science or related field

Tools

MS Word

Excel

Outlook

Job description

Worldwide Clinical Trials is seeking a Site Contract professional in the United Kingdom to draft, negotiate, and finalize site contracts and investigator agreements in alignment with budgets and study timelines.

You will review study budgets, liaise with Worldwide Legal and regulatory teams, and support cross-country approval and execution processes. Strong English and MS Word/Excel/Outlook proficiency are essential.