Christopher Mattair Email & Phone Number

Binghamton, New York, United States

Houston, Texas, United States

Houston, Texas Area

Manage 5 Core Lab projects; each project involves the collection of echocardiograms at external sites, the receiving and reading of these echoes by our study team and the creation and dispersal of various reports based on the scan data. Supervise external site work to ensure research study protocol guidelines are being followed, deadlines are being met and that quality data is being collected. Meet regularly with research sponsors to discuss study progress; we update study documents, contracts and manuals. Responsible for the monthly invoicing of study work. Collaborate with departmental and institutional financial analysts to write study budgets, contracts, Core Lab invoices and ensure correct billing of research patients.Coordinate(d) 12 Cardiology non-treatment trials, 3 Cardiology treatment trial and 13 cardiovascular treatment trials. Locate and recruit potential study participants from both inpatient and outpatient hospital clinics. Co-leader of a departmental 'Procedure Improvement Committee' that meets regularly to address and fix procedural areas of improvement within the department. Schedule and order scans (MRI/CT), procedures and blood draws for research patients. Collect protocol-required data from paper medical charts as well as electronic medical records (EPIC, Athena, Method) Compose regulatory submissions for our Institutional Review Board: continuing reviews, research protocol amendments, safety report submissions and deviations. Write/edit study informed consent forms and other study regulatory documents. Train and mentor new research coordinators (4) and study technicians (15+) on all relevant research policies, procedures and their role in the research process.

Houston, Texas Area

Coordinated numerous research-industry-sponsored and investigator-initiated kidney, prostate and bladder research trials. Collected study data from electronic and paper medical records and entered data into electronic case report forms.Worked with research nurses and investigators to prepare interim analysis statistical reports, reports centered on study drug toxicity and enrollment reports. Member of a committee that created and modified departmental operating procedures. Developed a patient tracking system used for data entry and adapted by the department for use with the auditing of external sites. Reviewed periodic reports about serious drug side effects from other research sites and worked with regulatory coordinators and investigators to update the informed consent forms as appropriate. Prepared Institutional Review Board continuing reports.

Dallas, Texas

Remotely supervised external-site IRB submissions and data collection to ensure regulatory compliance and data quality for 15 cooperative studies. Composed or edited all departmental informed consent forms, protocols, HIPAA forms and project summaries. Coordinated all institutional review board submissions, safety committee submissions and the completion of various reports for the trial sponsor. Represented my department on an institutional team guiding development of a new electronic medical record system as well as a new electronic IRB system. Hosted internal/external monitors during periodic visits and maintained communication afterwards to help maintain data integrity. Responsible for reviewing each new study protocol and preparing each new study start-up at both UT Southwestern and external sites. Screened and consented patients for possible participation in departmental research. Delivered instructional presentations for research personnel to demonstrate new regulatory procedures.

Master Of Business Administration - Mba, Leadership; Finance, 3.95 Gpa

Bachelor'S Degree, Psychology