Investigator Site Contracts Manager

Albion Rye Associates; Greater London; On-site; GBP 90,000 - 120,000; Full time

Job summary

Albion Rye Associates is seeking an experienced Investigator Site Contracts Manager to lead site contracting for complex international clinical trials and multi-protocol programmes in London. You will own strategy, negotiate investigator site agreements, grants and budgets, and support international study teams with regulatory and quality compliance.

The role requires strong GCP/ICH knowledge, a track record of handling high‑level negotiations with senior sponsors and stakeholders, and the

Qualifications

• 7+ years’ clinical site contracting experience within a CRO or pharmaceutical environment.
• Strong international investigator site contracting experience.
• Excellent contract and budget negotiation skills.
• Strong knowledge of GCP/ICH and the clinical trial environment.
• Experience managing complex, international studies and senior stakeholders.

Responsibilities

• Developing and delivering site contracting strategies
• Negotiating investigator site agreements, grants and budgets
• Providing specialist contracting support to international study teams
• Working closely with sponsors and regional stakeholders
• Ensuring contracting activities meet regulatory, GCP/ICH and quality requirements
• Monitoring timelines, performance and financial objectives
• Providing technical guidance and mentoring to colleagues

Skills

Clinical site contracting

International negotiations

CRO/pharma experience

GCP/ICH knowledge

Budget negotiation

Job description

12 month contract

We’re supporting a global organisation within the clinical research sector with the appointment of two experienced Investigator Site Contracts Managers for an exciting contract opportunity.

This is a senior-level role focused on leading site contracting activities across complex international clinical trials and multi-protocol programmes.

You’ll be responsible for:

• Developing and delivering site contracting strategies


• Negotiating investigator site agreements, grants and budgets


• Providing specialist contracting support to international study teams


• Working closely with sponsors and regional stakeholders


• Ensuring contracting activities meet regulatory, GCP/ICH and quality requirements


• Monitoring timelines, performance and financial objectives


• Providing technical guidance and mentoring to colleagues

What we’re looking for:

• 7+ years’ clinical site contracting experience within a CRO or pharmaceutical environment


• Strong international investigator site contracting experience


• Excellent contract and budget negotiation skills


• Strong knowledge of GCP/ICH and the clinical trial environment


• Experience managing complex, international studies and senior stakeholders

This would suit an established Site Contracts Manager / Clinical Contracts Manager who is comfortable taking ownership of complex international contracting activity.

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