Researcher, Investigator & Site Services

Choose one of the three or any combination from the suite of 'Get Me' programs and experience the strength of having a dedicated research team assist you in getting the clinical studies, research funding and patients you need to start and finish your studies.


The Get Me Research Funding^TM (GMRF) program was developed to assist researchers in acquiring study funding which is often difficult, time consuming and requires having the right connections. Subscribing to the GMRF program can reduce the time it takes to find the right sponsor for your research study.

Our years of experience in sourcing, initiating, organizing and managing research studies has allowed us to build strong connections with leading government, not-for-profit and private investment research funding organizations and sponsors of various research studies.

In addition to our month-to-month subscription payment options; we also offer a variety of creative partnering models and customized fee-for-service arrangements from straight consulting, brokering, shared gains-risks agreement, and royalty fees from a performance-based model of payment.

To get started and take advantage of our one month trial offer, just fill out our Online Research Information Form below and let us find you the funding you need for your projects.

                        Online Researcher Information Form



This affordable monthly subscription program is dedicated to finding and delivering to you the studies you want. The process is cost efficient and effective.

This is how it works:

1. The Get Me Clinical TrialsTM research team will send you a weekly report of active and soon-to-be enrolling clinical trials from our Clinical Trials Database. 2. You select the studies you are interested in pursuing, and 3. We will send you study start-up documents such as CDA, Protocol Synopsis and Site Information Questionnaires for each enrolling study. Partnering with our GMCT study start-up specialists is like having your own dedicated study acquisition team working to find clinical trials for you day in and day out. We offer selective or comprehensive patient recruitment services from our Get Me Research PatientsTM(GMRP) program that helps you get the exact patients that you need for your studies. The GMRP is anchored by our proprietary VALIDATE System® - a de-identified patient recruitment database searchable by your protocol's inclusion/exclusion criteria. Exodon's time-tested 6-Point strategy and approach to patient recruitment includes the following solutions: Our VALIDATE System® patient recruitment database program identifies and matches patients in your area with the study's inclusion and exclusion criteria. In addition to we also offer other effective patient recruitment solutions including: Patient screening centers Patient referral centers Site-based patient recruitment Direct-To-Patient recruitment Media-based recruitment Public relations & media-based recruitment Our 6-point program can help deliver the patients you need for your studies. Contact Us to find out more about these services.

For more cost savings we offer our 'Get Me' bundled offer. Select all 3 of the 'Get Me' programs' and receive up to a 40% discount

Exodon's Site Management Organization (SMO) and Trials Management Organization (TMO) Network of Sites

Despite a growing number of researchers participating in clinical research studies, approximately 70% of clinical researchers who have conducted 3 or fewer sponsored trials will not continue conducting clinical trials.

As investigators can attest to; there are many reasons for this high rate of investigator attrition. Insurmountable paper work, adversarial relationships with site monitors and declining reimbursement are among the top reasons many clinical research sites stop conducting studies.

According to a white paper published in June 2002 by IBM Global Industries, a paradigm shift in clinical trial research is long overdue. The clinical trial research process needs to become more efficient and more effective; but how? In that white paper - a three tiered solution was proposed:

1) The process of identifying potentially interested patients who are appropriate for a given study needs to become more automated;

2) More GCP/ICH trained researchers and more research subjects are needed;

3) A successful partnership between clinical research companies with site and trial management expertise and investigators is needed that ultimately reduces the site's burden in clinical research tasks such as patient recruitment, contracts, and regulatory affairs.

At Exodon, we have created partnerships with clinical research investigators - through our Validate System® network of sites. This is a database platform that matches the site's metrics and their patients to ongoing and upcoming trials.

What is the VALIDATE System® Network of Sites?

This system validates that a site has the ability to conduct the trial and has pre-consented patients meeting any given study's inclusion/exclusion criteria virtually eliminating most study screening failures and patient recruitment bottlenecks.

We firmly believe in order to make the clinical trial research process more efficient, effective and rewarding to the investigator, clinical research support, particularly in the area of patient recruitment, is required for the site well before the research protocol is accepted by the investigator.

We partner with our doctors at the most critical level - their medical practice. We offer our investigators patient recruitment tools that include both paper based and electronic medical record solutions. These solutions enhance our doctors' ability to more accurately identify their patients' eligibility to participate in clinical research.

As the information from each investigator and/or their patient records are de-identified and imported into our VALIDATE System® database, their patients are pre-consented and are available to participate in upcoming research. We as well as other CROs, Pharmaceutical and other study sponsors worldwide use this database to complete their studies. Exodon then brings these studies to our TMO and SMO sites at no on-going costs.

We realize there are good reasons why so view clinicians conduct clinical trial research. So in addition to our technological solutions, Exodon offers other clinical research support services beyond automating and marketing your clinical research practice and offer if needed:

Investigator and clinical coordinator training services

Study start-up and site management support

Per diem on-site clinical research staffing including CRC and Study Mangers

Contract and budget negotiation support services

We welcome you to come join our growing family of over 300 affiliated investigators worldwide and make clinical research a significant part of your clinical practice.

To get more information or schedule a meeting
click here to Contact Us

To enroll in the VALIDATE System® Network of Sites as an affiliate of Exodon use our

Online Investigator Enrollment Form or
Online Clinical Research Agreement Form