Site Management and Clinical Monitoring

Our experienced Regional Site Managers (RSMs) are recapturing the importance of building relationships with our clinical sites that empower efficient site management and monitoring. Our RSMs are therapeutically-aligned with our clients’ program and can act as a “one-stop shop” for all activities related to a clinical study site.

Overview of expertise:

  • Site identification and feasibility
  • Start-up activities including IRB submissions, essential document collection, and contract and budget negotiations and approval
  • Site qualification visits, initiation visits, routine monitoring visits, and closeout visits
  • Source document verification and remote monitoring
  • Site management including enrollment, serious adverse event reporting, essential document maintenance, and study updates
  • Study site and Investigator payment administration and management