SITES NEEDED FOR ASTHMA, COPD, RSV, COVID OUT-PATIENT, PTSD, AND DMII. CONTACT US NO
BlueCSO by Blue Consulting Group
About US
Who we are?
BlueCSO is a Clinical Site Organization that bridges the gap between the Clinical Research Site, Clinical Research Organization, and Sponsor. We are a team of experienced certified professionals that are here to assist your clinical site to carry out your studies effectively, in accordance with FDA regulations, while you maintain the ability to focus on our medical heroes, your research patients.
How We Help
At BlueCSO, there are an array of services offered for the site level for a fraction of the cost of in-house Research staff. Our services include but are not limited to: Study Brokerage, Site Feasibility, Contracts and Budget Execution, Site Initiation, Protocol Writing, Source Document Creation, Quality Assurance, Clinical Operations, Regulatory Affairs, Remote\In-House Coordination, Coordinator Staffing, Data Entry, and Sponsor Invoicing,
Sign up to be included in our current study list
Our Services
Regulatory Management
From study start up to close-out, BlueCSO offers a dedicated regulatory manager to be the liaison between your clinical site and sponsor. With 48-hour turn around for all regulatory request, ISF and eISF Management, and IRB submissions expect to standout to your protocol stakeholders. Your dedicated regulatory manager with support your every needs.
PI | Sub-I Placement
Looking to expand? Our Physician Recruiters will find the right PI for your site!
Staff Placement and Training
Having trouble hiring?
Let our recruiters find the right staff for you; once onboarded they will go through a three-week site-specific coordinator training.
CTMS and Project Management Software
BlueCSO offers a CTMS and Project Management System that fits all of your site needs. No need to have multiple vendors for operations.
PCO at Home Research
We understand sometimes patients just can't make it into the office let our at home coordinators and laboratory technicians take care of your visits for you. No more out of window visits!
Site Start-Up
Are you ready to bring innovative treatments to your community and patients? BlueCSO offers full start-up assistance. Let us dot your I's and cross your T's to make sure you maintain compliance.
Study Brokerage
Getting studies are hard! We have partnered with the leaders in study feasibilities! Sign up today to access our study lists. Lists are updated weekly.
Contract and Budget Negotiation
Are you being compensated correctly for your studies? Let us negotiate your budget in a 48-hour turn around at 30% overhead.
Source Document Creation
Details... Details... Details...
Let us create your sponsor approved source documents and send them right to your door!
Data Entry
Your coordinators need to focus on recruitment and the care of your medical heroes, and our sponsors need quality and timely data. Let us take care of your data entry with our 24hour specialist through BlueQR.
Quality Assurance
You always need an extra eye, let our specialist handle quality assurance. Our QA program can be specific to your site starting with daily source review, monthly on-site monitoring visits with our in-house CRAs, medical history review by our medical doctor, and mock audits from previous FDA inspectors.
Reviews
This website uses cookies.
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.