Administrative Office: C621 GH

Purpose:

Protocol development (writing/editing), scientific and safety peer review, study administrative monitoring, and Oncore administration is the responsibility of the Office of Clinical Trials Development Support and Monitoring (CT-DSM). The CT-DSM collaborates with the CTSC in providing infrastructure for HCCC clinical investigators.

Services provided include:

1. Protocol writing and editing
2. Coordination of biostatistical consultation with the Biostatistics Core
3. Development of data and safety monitoring plans
4. Bi-annual and quarterly safety audits
5. Administrative support of the PRMC and DSMC
6. Communication with regulatory offices for oversight of clinical research
7. Oncore Administration and Training

Contacts:

Gary Rick, MSW
Protocol Administrator
319-353-7846
gary-rick@uiowa.edu

Meggan Fisher
PRMC Clerk
319-353-7252
meggan-fisher@uiowa.edu

Marilyn Rosenquist, MS
Protocol Writer/Safety Officer
319-353-7899
marilyn-rosenquist@uiowa.edu

Thomas Noonan
Clinical Trials Application Developer
319-356-4535
thomas-noonan@uiowa.edu

Brian Smith, PhD
Biostatistician
319-384-5026
brian-j-smith@uiowa.edu

Gideon Zamba, PhD
Biostatistician
319-384-5020
gideon-zamba@uiowa.edu