Become an Investigator with ICRC

Fill out the Investigator form and email your CV

Physicians who are interested in being an Investigator should submit a signed and dated curriculum vitae (CV).

Meet virtually or at your office

We will review your clinic and provide a startup site questionnaire. Our team will customize our research model to fit your clinic's specific needs and services, and answer any additional questions.

Begin your trial

Let us take care of the study management services and handle the paperwork for you. With ICRC by your side, you can focus entirely on your patients. Our team will assist you in patient recruitment by searching your EMR or running advertising campaigns to promote the trial and your practice.

Onboarding a study

We will meet to discuss the types of trials you are interested in, sign confidentiality and investigator agreements, and begin obtaining trial leads.

Clinical trials are a viable care option for individuals seeking treatment.

Are you interested in providing your patients with additional treatment options and preserving your clinic’s independence?

  • We offer a reliable research structure that is customized to suit your practice's specific needs.

  • Our study management services will take care of the paperwork for you, giving you more time to focus on your patients.

  • We also provide patient recruitment services, whether it's searching your EMR or advertising the trial and your practice..

Participate in clinical trials without the need for additional staff.

The opportunity to expand treatment options, increase access to healthcare, and generate additional revenue without extra staff or financial burden to the practice.

ICRC provides:

  • Study acquisition

  • Document handling

  • Patient management and scheduling

  • Experienced research staff

  • All study-related equipment and supplies

We align you with clinical trials tailored to your practice’s needs and preferences.

ICRC collaborates with physicians to provide patients with optimal therapies.

Our team creates customized marketing materials for each study or practice, utilizing various techniques, including personal referrals and advertising on social media, local papers, and radio/TV.

Site Management

Our Site Management Organization (SMO) service is a comprehensive solution for clinical trial sites. We provide consultation towards facility management, staffing, operational training, and regulatory support services to ensure clinical research success. Our team of experts assists with site feasibility submissions, identifies the best clinical site locations, and provides top-notch clinical support staff to enhance the availability of new medication. With our SMO services, you can be confident in the success of your clinical trials.