We offer broad site management services to support, monitor and manage sites during all stages of a clinical trial beginning from feasibility to closure.
Site Feasibility, Selection, Qualification
We simplify the process of evaluation and selection of sites in respect to all the relevant aspects including site infrastructure, staff credentials, ethics and regulatory.
Site Budget and contract negotiation
We have a dedicated project management team with customizable processes and workflows to take care of all the complex issues that may come up during budget and contract negotiations.
We use various methodologies to run smooth and efficient training programs for site personnel that ensure compliance with GCP, Protocol, ethical and regulatory requirements.
Start up and activation
We develop tools, materials, and trackers necessary for all Site Level regulatory documentation and procedures leading to site activation.
Our experts provide the tailored essential documentation checklists to the site and support the site in creation and completion of these documents including but not limited to Informed consent forms.
IRB submissions, annual reports
Our experts can help create the submission applications and checklist and even submit to the IRBs on site’s behalf. We also provide all the backend support and templates required for IRB submissions and annual reporting.
Our project managers have expertise in creating site specific budgets and payment schedules. All the site and patient payments can be automated with the use of the budgeting solutions.
Cereblis enables companies to take advantage of innovation in tech by onboarding new ways to work and execute projects by advising, implementing, and optimizing digital solutions.
Cereblis LLC, 1770, Park Street,
Suite 108, Naperville IL 60563.