University of miami clinical trials

Content can also be filtered down to relevant studies run by investigators from a specific department, facility, center, or division as available. This tool uses content already available in University of Miami enterprise research systems.

As a result, changes and formatting of the content in those systems will affect the content in the CTST. Sponsored studies that have an associated NCT number are also eligible. Some sponsor agreements restrict public disclosure of their affiliation with the institution. Investigators and study staff interested in taking advantage of this tool should work with the CRIS office as needed to make sure their study is not violating any confidentiality provision.

The primary study contact is the primary clinical research coordinator for the study. Make sure your protocol is up to date with any changes and the correct staff member is the primary contact in Velos. Typically this is done at the departmental, center, or division level.

Study coordinators can transfer calls to another number. If all studies within a group need to reference a different central phone number, contact resinfo med. ORIM will work with your department, division, center, etc to determine an appropriate solution. The phone numbers associated with individuals in the study result screen are taken from the human resources system for the University. Ensure that the HR system is up to date with the correct phone number.

Changes should appear in the CTST within 48 hours. If you have further issues with this, contact resinfo med. If you don't have an NCT number, but CRIS has confirmed that your industry study can be promoted publicly, forward a communication from the CRIS office notifying us that it is fine to publish the study in the tool, copying the CRIS office on the message, to resinfo med. This feasibility review should include a financial review, consideration with respect to available technical and personnel resources and sufficient patient pool, as well as any third party required deadlines assessing whether the University of Miami can initiate the Clinical Research project within that specified deadline.

To assist with the financial portion of the feasibility review, please click here for the Clinical Budget Checklist and here for the Study Budget Template. The CRIS fee is a one-time fee charged to all industry-supported studies. This is a mandatory, non-refundable, central office fee that applies to all new projects and any amended projects that were not assessed the fee originally.

Below you will find links to additional information related to the initiation of a Clinical Research project. When initiating Clinical Research at the University of Miami, you will need to also communicate and work with the following offices:. Clinical trials are research studies that involve people. They are the final step in a long process that begins with research that is done in a lab. Clinical trials are key to developing new methods to prevent, find and treat all types of diseases.

It is through clinical trials that scientists can find out if new treatments are safe and effective and work better than current treatments. Need help finding a location? Near by icon--use-location Created with Sketch. Use my current location.