• Prepares and submits regulatory documents to sponsors, CROs, UT Health IRB, and local andcentral laboratories.• Completes feasibility questionnaires for potential trials; works with sponsors on study start-ups, closures and budgets.• Coordinate subject recruitment in house and at various outlying clinics.• Submits SAE and IND reports, protocol violations and deviations, as well as updates to study safety information (Investigator Brochures, Audit and Monitoring reports) in accordance with IRB reporting criteria and timelines. • Submits study continuing reviews and amendments to IRB.• Responsible for research billing reporting for all studies.• Maintains master regulatory document files for multiple studies simultaneously. Prepares documents for SIV’s, monitoring visits, and closures.• Revises Informed Consents based on protocol amendments before submission to IRB for approval.• Creates and updates FDA 1572 forms; trains and supervises personnel regarding IRB procedures.

UT Health Research Assistant for Physical Medicine and Rehabilitation department

* UT Health Research Coordinator is housed in TIRR Memorial Hermann.* All studies follow TIRR SOPs for scheduling and labs.* Experienced using Memorial Hermann's EMR system (Care4).

Design structured cardiovascular and resistance training programs, diet plans as well as focus on specific problems (i.e. injuries, obesity, etc.) for gym members.