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

 

EXPERIENCED REGIONAL CLINICAL SITE MANAGERS

Clinical Site Managers at ACE 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.

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