The purpose of Ancilla Services, LLC is to connect Sponsors and CROs with the investigators and sites who are able to successfully conduct a specific clinical trial. We work alongside our clients throughout the feasibility and site selection process to ensure that their site capabilities match with protocol requirements. This results in success for the sponsor, CRO and the site. There is no cost to the sponsor or CRO for our services.

We specialize in providing clinical research support services to physician groups and research facilities including business and study pipeline development, regulatory and quality assurance, contract and budgets, site management and QA, and patient recruitment and advertising support. By making these services available to our sites we are able to effectively manage the growing demands of conducting clinical trials.

We have a solid infrastructure and experienced staff that have positioned us to provide all of our partners – physicians and pharmaceutical companies – with quality, outcome based clinical trials.

All sites are able to perform study-related tests and procedures on site or within close proximity and have adequate monitoring areas with internet access. All of the Ancilla Services sites are able to use a central IRB and are experienced with various EDC systems.

We ensure that our clients have a history of meeting or exceeding enrollment goals with high retention rates and quality data.  Each Ancilla Services site has experienced, dedicated, full-time research personnel and actively involved investigators.

If you would like information on any of our sites, please do not hesitate to contact us for more information.

Program Development for Clinical Research Sites

Ancilla Services