Revitalizing Struggling Sites - The Site Rescue Advantage

Initial Consultation

Step 1: Physicians, CROs, and Sponsors interested in ICRC's site rescue service should complete the contact form. We will then schedule a brief call to understand your site’s specific challenges and goals.

Site Performance Review

Step 2: We will evaluate key aspects of your site’s operations, including compliance, patient recruitment, staff training and overall efficiency.

Implementation and Rescue Plan

Step 4: If you decide to proceed with our site rescue services, we’ll develop a tailored support plan that ensures your site’s long-term success.

Actionable Recommendations

Step 3: You’ll receive a summary of findings and customized recommendations on improving site performance, enhancing compliance, and streamlining trial execution.

The Clinical Trial Challenge

  • Around 80% of trials fail to meet the initial enrollment target and timeline, leading to delays that result in lost revenue of up to $8 million per day for drug development companies (source).

  • Regulatory compliance issues increase Sponsor risk and potential trial failures.

  • Sites with poor operational efficiency drive up costs and prolong study timelines.

  • Sites struggle with staff turnover, lack of expertise, and operational inefficiencies.

How ICRC Helps - Our Site Rescue Approach

Sponsors and CROs:

  • Regulatory Compliance and Audit Readiness - Ensuring adherence to GCP, FDA, and Sponsor requirements.

  • Trial Acceleration Strategies - Identifying and optimizing struggling sites for better performance.

  • Risk Mitigation - Reducing protocol deviations and non-compliance risks.

Sites:

  • Staffing and Training Support - Deploying experienced CRCs, CRAs, and site coordinators to stabilize operations.

  • Patient Recruitment and Retention - Implementing strategic enrollment solutions to accelerate recruitment

  • Operational Efficiency and Site Performance Management - Optimizing workflows to reduce delays and deviations.

Key Benefits of Partnering with Us - For Sponsors and CROs

  • Faster study timelines and improved trial success rates

  • Reduced site failures and costly delays

  • Enhanced regulatory compliance and site oversight

Sites:

  • Increased patient recruitment and retention

  • Better-trained, experienced staff to ensure operational success

  • Long-term sustainability and new trial opportunities

Let’s Connect!

Looking to enhance site performance or rescue underperforming trials?

Contact us today to discuss how we can optimize your trial sites and support your clinical programs.