Clinical investigators who are responsible for conducting clinical trials can rely on MedTrials to help them navigate through heavily regulated research requirements. MedTrials clinical trial management experts are an excellent resource for investigational site personnel by offering consultation, staff and operations development as well as compliance support services.

Please contact us if you are interested in support services or trial opportunities. We encourage all sites to register in our investigator database by submitting the information requested in the following link or simply submit your CV to [email protected].

* First Name

* Last Name

* Email

Phone

Web Site

Institution/Study Site Name

State

Street Address

Address Line 2

City

State / Region / Province

ZIP / Postal Code

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Degree/Qualification:

Other Qualification:

Primary Medical Specialty:

If other, please specify:

Previous Clinical Research Experience:

Number of years conducting clinical trials as a Principal Investigator:

Number of years conducting clinical trials as a Sub-Investigator:

Clinical Trial Experience:

Have you conducted :

Phase I trials:

Yes

No

Phase II trials:

Yes

No

Phase III trials:

Yes

No

Phase IV Trials:

Yes

No

Is your site part of a Site Management Organization:

Size of research staff (# of personnel):

Central or Local IRB:

Do you have previous experience with MedTrials?:

Yes

No

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