Dorisca Research Consulting LLC
Dorisca Research Consulting LLC
  • Home
  • Services
  • Our Network
  • Clinical Trials
    • About
    • Dermatology
    • Pain Management
    • Gastroenterology
    • Internal Medicine
    • Opthalmology
  • Investigator Inquiry
  • Contact
  • Sign Up!
  • More
    • Home
    • Services
    • Our Network
    • Clinical Trials
      • About
      • Dermatology
      • Pain Management
      • Gastroenterology
      • Internal Medicine
      • Opthalmology
    • Investigator Inquiry
    • Contact
    • Sign Up!
  • Home
  • Services
  • Our Network
  • Clinical Trials
    • About
    • Dermatology
    • Pain Management
    • Gastroenterology
    • Internal Medicine
    • Opthalmology
  • Investigator Inquiry
  • Contact
  • Sign Up!

Investigator Inquiry

There's much to see here. So, take your time, look around, and learn all there is to know about us. We hope you enjoy our site and take a moment to drop us a line.

Sign Up

Services

Client Services

Nature of Services

Clinical Trial Management

DRC, LLC will provide access to new clinical trials every Month as well as complete management of the Startup Process up to SIV.

Contracts and Grants Management

DRC, LLC will handle the Contract & Budget Review for all New Clinical Trials

Industry Sponsor Budget Negotiation

DRC, LLC will negotiate the budget with sponsor to cover all study related site cost.

Invoice, Billing and Collection

DRC, LLC offers Study Startup and Visit completion invoicing on all projects.


Ancillary Services

Ancillary Services

Financial Assessment/Monthly Billing

Tracking and documenting completion of all study related visits to assess earned revenue and then invoicing the sponsors monthly to ensure that all funds are received at your site timely and correctly. 



Pt. Stipend Review & Prep

Generally all patients will be paid a stipend for their participation. DRC, LLC will issue each patient a debit card loaded with the funds that is owed to them. DRC,LLC will prepare the account, issue the debit card and load the debit card per completed visit for the patient.


Continuing Review

DRC, LLC will prepare and submit the required annual report to the IRB, updating them about your study progress. 

Internal Study Audit

DRC, LLC will audit your site to make sure that all clinical trials are being processed correctly and all documents are in order.

Sponsor Study Audit

If the sponsor wants to come audit your site, DRC, LLC will review your study to make sure that all aspects of the clinical trial are in order.

Contract Amendment/Updates

If your contract ever needs to be amended, DRC,LLC will take care of the negotiations.   DRC, LLC performs an internal analysis to determine all study related costs, then negotiates directly with the study sponsor for the support that is needed.

Offsite Data Storage

DRC, LLC will take care of packaging, labeling and shipping of all study related documents for your practice. 



Study Coordinator Assignment & Training

DRC, LLC will provide a research study coordinator at your site to manage the required clinical trial visits.  If you have a potential coordinator at your site already, DRC, LLC will train any of your nurses to be a study coordinator.

Study Close Out

Once the study is over, the sponsor will need to conduct a closeout visit. DRC, LLC will look over your study documents and make certain that all documentation is complete, in preparation for the closure of the study.

Department Infrastructure Development

DRC, LLC will assist in the development of your research department at your site.  DRC, LLC will meet with you and determine the types of trials that your research department would like to conduct and assist in the preparation of your department to accept the clinical trial.


DRC, LLC will walk your site through the Site Qualification Visit in order to provide support in obtaining your first clinical trial.


Consulting

Consulting Services

Account Reconciliation & Closure

For completed Trials

Account Reconciliations and Billing

For all active Trials

Existing Clinical Trial Budget review

For appropriate coverage of study costs

CTMS

Review current Clinical Trials Management System and make suggestions for improvements

Development of Institutional Overhead Rate

 Research related

Master Agreement & Fixed Costs

* Make suggestions for CTA standard verbiage (Master Agreement) and standardize fixed costs pertaining to the study budget.

Define Process

 Clinical Trial Lifecycle workflow

Instruction Manual For Staff

Working Instructions Manual for staff

*Please Contact Us For Pricing

Social

Copyright © 2025 Dorisca Research Consulting LLC - All Rights Reserved.

Powered by