Novel Methodologies and Pilot Studies
Awards for Innovative Clinical and Translational Research
Funding Opportunities for Innovative Clinical and Translational Science at UAMS
The overall goal of the TRI is to transform the pace, effectiveness, and
quality of translational research among UAMS and its partners, resulting
in better health for all Arkansans. The TRI funding programs intend to
1) facilitate research innovation and progress, 2) stimulate and
solidify research collaborations and 3) promote high-quality
translational research. Awards are intended to support novel research
studies; these awards will not support projects that are minor offshoots
of ongoing research or provide bridge funding to investigators.
The awards encourage investigators to develop research programs that
successfully compete for extramural funding. The TRI will support
investigators by providing guidance, resources, and feedback. Please see
below for the available funding mechanisms and full RFAs.
Visit our FAQ page for answers to commonly asked questions about the TRI Pilot Studies program.
RFAs Available
The TRI is currently offering the following award mechanisms:
Annual TRI Pilot Research Awards in Clinical and
Translational Science ($50,000, one year of funding)
Instructions for the Pre-proposal
Deadline: April 6, 2012
Instructions for the Full Application (Invited Applications only)
Deadline: May 31, 2012
Targeted
Awards For Innovative Clinical and Translational Research -
Focus: Drug and Biologics Development (1-3 awards, 200,000 total
available).
Instructions for Applicants
Deadline: March 21, 2012
Grant Forms
These forms are to be filled out, saved, and submitted along with invited grant proposals.
Milestones and Evaluation Table (Word .doc)
INNOVATIVE CLINICAL AND TRANSLATIONAL RESEARCH AWARD
The UAMS Translational Research Institute (TRI) invites applications for TRI Drug and Biologics Development (DBD) Awards. The TRI expects to fund 1-3 DBD Awards up to a total of $200,000 and will provide one year of funding. Fundable projects and their budgets may vary significantly, depending on the needs of the applicant. Examples may include smaller projects requesting licensing/legal support to move projects toward FDA approval and Phase I trials, support to complete key toxicological or teratological studies to file INDs with the FDA, or larger studies supporting key trials in humans that will significantly and quickly advance the PI's work. Early stage drug and biologics development, such as screening to select new medications, will not be considered.