Global Considerations

We help sponsors select sites with capabilities to fit a specific protocol for efficient study startup. We identify a site’s experience with study-specific procedures, access to the target patient population, recruitment plans and supported screening, and enrollment projections.

We select regions where disease to be studied is prevalent.
We consider standard of care.
We avoid sites saturated with clinical trials.

Contract negotiations

Our Clinical Solutions Contracting Team will use Sponsor Contract Templates and pre-approved contract language to execute site contracts and get your trials up and running. While managing sites, ACE Researvh provides prompt reports to you and timely payments to your sites. Site reimbursement can be defined for enrollment based upon anticipated resource utilization for each protocol and non-standard of care procedure charges. Payment will be made to sites based on predefined milestones as set forth in the Clinical Trial Agreement (CTA) for each project.

Obtaining Confidentiality Agreements
Budget Negotiation
Executing Site Agreements
Negotiating Site Contracts
Committee Member, Site, and Investigator Payments

Site management services

We offer the following site selection and management services:

Site training
Subject Recruitment and Retention
Standard Operating Procedure (SOP) Development
Development of Clinical Trials Materials

Need help setting your next clinical
trials for success in Africa?

We can help with Protocol design, Regulatory affairs, Site selection, Clinical monitoring, Site management, Data management & much more.
Please fill out the Form below

Expand your practice and build your career with
clinical research.

ACE Research is always seeking to expand our network of principal investigator partners. If you are interested in participating in clinical research, we offer the opportunity to join an accomplished investigative clinical research team.
Please fill out the Form below