Services for Investigators

 Apex Clinical Trials, LLC (Apex) is a Trial Management Organization (TMO) conducting phase I-IV, out-patient medical, psychiatric (CNS), medical device and combined product clinical trials in geriatric, adult, and adolescent patient populations for the pharmaceutical, biotechnology, medical device and combined-product industries in the United States.

Apex offers new studies to investigators with centralized CDA, feasibility, budget, contracts, regulatory submission to sponsors & CRO’s globally including complete patient recruitment. We also provide study coordinators and support infrastructure set up.

Apex provides the Investigator/Investigator Site with the following services with 24/7 help line:

• Complete study management
• New clinical trials
• Study coordinator as required
• Centralized CDA & feasibility submissions and management
• Pre-study site visit (PSSV) package, scheduling and management
• Centralized budget & contracts negotiation and management
• Centralized regulatory affairs submissions and management
• Site initiation visit scheduling and management
• Complete patient recruitment with patients phone screened and scheduled for each study
• Monitor visits scheduling and management
• Close-out visit scheduling and management
• Payment to principal investigator/investigator site with various options.

 Contact Us with any questions you may have.