CLINICAL TRIAL SITE MANAGEMENT

A competent site manager is essential for the success of your clinical research in Africa.

Clinical trial site management can be a complex and challenging task.

• Every site possesses its own set of SOPs and distinct levels of expertise and experience.
• Infrastructure capabilities can vary significantly.
• It’s possible that people may have different communication styles.
  

This can lead to unclear communication and responsibilities, protocol procedures being misunderstood or implemented correctly, and communication delays.

Access 100+ Sub-Saharan Africa Sites

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EXPERIENCED REGIONAL CLINICAL SITE MANAGERS

Clinical Site Managers at AXON Research serve as single-point coordinators, building strong site relationships and ensuring your clinical research is safely, ethically and executed efficiently.

Our site managers responsibilities include:

• Recruit and train sites on ICH-GCP and SOPs.
• Manage RACI and timelines.
• Equipment and supplies inventory management.
• Communication and issue escalation
• Support AE, SAE, AESI and general safety reporting.
• Audit and inspection readiness.
• Sample validation, reconciliation and shipment

Elevate your clinical trials with our expert clinical site management services.

WHY CHOOSE AXON RESEARCH SMO

We offer one-of-a-kind Site Management Organization (SMO) services improving relationships with African research sites and investigators and facilitating effective site-sponsor interactions.

• Simplified, centralized access to multiple sites.
• Staffing – Hire, train and compensate site employees
• Centralized PI/site training – Protocol, SOPs, GCP
• Centralized Study Start-Up and CTAs
• Dedicated patient recruitment professionals.
• Clinical supplies inventory management from a single interface.
• Standardize SOPs and quality metrics
• Scientific and resource support for investigator-initiated trials
  

TACKLING INEFFICIENCIES IN SITE MANAGEMENT

The Conventional Approach to Site Management is fragmented

This leads to increased sponsor oversight, prolonged timelines, increased costs, and potential risks to patient safety and data integrity.

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Make a difference in patients’ lives by setting your clinical trial on the path to success today.