The Department of Pediatrics and the School of Medicine offer several opportunities to assist faculty in the development of research projects. To learn about the grants and programs available, click through the tabs in this section. Resource links are also available under the "Training and Funding Links" section on the right hand side of the page.
The Carolina Postdoctoral Program for Faculty Diversity
As part of a continuing commitment to building a culturally diverse intellectual community and advancing scholars from underrepresented groups in higher education, The University of North Carolina at Chapel Hill Carolina Postdoctoral Program for Faculty Diversity is pleased to announce the availability of postdoctoral research appointments for a period of two years. The purpose of the Program is to develop scholars from underrepresented groups for possible tenure track appointments at the University of North Carolina and other research universities. Postdoctoral scholars will be engaged full-time in research and may teach only one course per fiscal year.
The program supports 10 postdoctoral scholars, engaged full-time in research and writing for a two-year term starting July 1. Fellows are provided in the program with research funds, program laptop, as well as department mentor, office, computer, health benefits and $39,874 annual salary. Meetings and workshops are structured for the purposes of networking, social interaction and supporting professional development of diversity postdoctoral scholars within the program.
If you have any questions or need further information, please contact Program Manager Judson Fraley in the Office of Postdoctoral Affairs at email@example.com. You can also visit the program web page.
N.C. Children’s Promise Research Grants
Thanks to efforts by Toni Darville, Wayne Price, and Terry Noah, the NC Children’s Promise (NCCP) Research Grant program has recently undergone changes to make it an even more exciting opportunity for members of the Department and the Children's Hospital.
Applications are now requested from Faculty and Fellows for a limited number of grants supporting pediatric-related projects. This program aims to assist new investigators in developing their research efforts and to provide support for established investigators with new projects or lapsed funding. Grant amounts range from $5,000 to $50,000.
For more details, contact Anna Martin.
In 2012, the APA launched a new research training program for APA members, modeled on their successful APA Educational Scholars program. This competitive 3-year program includes establishment of mentors (local and national), completion and publication of a research project and monthly webinars regarding clinical/translational research methods.
The Department of Pediatrics will consider supporting selected scholars for this program.
Please contact Terry Noah for additional details.
Department of Pediatrics Research Day
Pediatric Research Day is an annual event showcasing research by Department faculty. In 2011, the theme of PRD was multidisciplinary team research.
Research Day is currently organized by the Child Research Core of NC TraCS.
Contact George Retsch-Bogart for more details.
Multidisciplinary collaborations have moved to the forefront of biomedical research, as a more rapid pathway to translation of scientific discoveries to the bedside. Eliana Perrin, MD, MPH discusses research collaborations in a series of interviews for the 3-C Institute for Social Development, an RTP-based, NIH-funded company promoting social development research. Dr. Perrin is an Associate Professor at UNC and an NIH funded researcher in childhood obesity with extensive experience in multidisciplinary collaborations.
The Carolina Survey Research Laboratory (CSRL), a research unit within the Department of Biostatistics, provides state-of-the-art survey data collection methods that you can depend on. Our forty-five station call center is fully equipped to conduct CATI surveys, web surveys, and mail surveys, as well as focus groups and qualitative interviews. Our statisticians are capable of assisting you with questionnaire and survey design, sampling, nonresponse adjustments, complex data analysis, and multivariate modeling.
High-quality research requires high-quality study design, biostatistics and data management. A summary of the on-campus options for accessing biostatistical advice and support follows. In some cases, this may be associated with costs. Department of Pediatrics resources to help support will vary year to year but may be available. To request funds from the Department for biostatistical support, Faculty may submit an application form to firstname.lastname@example.org.
Faculty may submit requests for biostatistical support through TraCS here. A biostatistician group will review each request, ask any questions they may have, and then determine the best option, as follows:
- Walk-in clinics (no cost) – For general statistical questions or consulting.
- Overview (no cost) – General/broad advice from a biostatistician about a given research project.
- Seminar Series (no cost) - Provides junior clinical and translational researchers who have basic quantitative training in biostatistical methods with a more in depth understanding of selected topics and to introduce them to more advanced methods. Emphasis is placed on what is needed to understand a statistical method or concept in order to recognize whether a methodology is potentially relevant to their research aim and choice of study design, and appropriately interpret results of analyses using the methodology. For more information, contact NCTraCS_BiosSeminar@unc.edu.
- Group feedback (no cost) – If your data are complicated and routine analysis does not apply, faculty may present to a group of Biostatisticians at the Bios Core Grand Rounds and they will discuss the problem with you and provide you with suggestions. Depending on the problem, follow-up meetings with a subgroup of Biostatisticians are available. Contact Dr. Jianwen Cai.
- In-depth support (cost) – Fees associated with the in-depth support options are determined individually by a Professor in the Department of Biostatistics, and are based on each faculty member's need. Options for support are as follows:
- Biostatistician that oversees your work
- Biostatistician that does the work for small bursts throughout lifetime of project
- Biostatistician that is integrally involved in the project
- Biostatisticians can be written into a grant or contract, or the funds available through the Department of Pediatrics may be used to support some percentage of their time.
Biostatisticians from the Department of Biostatistics can be written into a grant or contract, or the funds available through the Department of Pediatrics may be used to support some percentage of the Biostatistician's and their programmer's time.
Biostatisticians at the CSRL provide expertise in sampling, questionnaire design, nonresponse adjustments, population-based weights, complex statistical analysis as well as data collection by telephone, Internet, mail or face-to-face. Free consultations are available.
For more information, call Robert Agans at (919) 843-5923.
Housed within the Department of Biostatistics, the CSCC is a data coordinating center for multi-site clinical trials and observational studies. The CSCC provides:
- Statistical collaboration on protocol design
- Design and implementation of a state-of-the-art electronic data collection and management system using the Carolina Data and Reporting Tool (C-DART) platform. C-DART is jointly developed by the CSCC and NC TraCS
- Multi-site trial project management, clinical site training and monitoring, database QC and cleaning, status reports, DSMB/OSMB reports
- Statistical analysis, manuscript collaboration, manuscript tracking for large studies, generation of public access databases
Biostatisticians and CSCC staff can be written into a grant or contract. Initial consultation may be arranged through NC TraCS, or by contacting Dr. Sonia Davis.
The Odum Institute offers walk-in, short-term and longer-term statistical, survey and data management consulting. The Institute also provides a range of short courses including quantitative and qualitative methods, survey research and data management.
For more information or to arrange a consultation, call the Institute's main line at (919) 962-3061.
Housed within the Lineberger Comprehensive Cancer Center (LCCC), the Biostatistics and Data Management Core is a no-charge facility open to LCCC members and those performing cancer research at UNC. The Core provides weekly walk-in clinics as well as individual consultation and support for:
- Research and protocol design, including implementation and programming of specific sampling schemes, the assistance in clinical protocol preparation, including the choice of proper design and statistical analysis methods, and the development of special software programs or macros for handling non-standard data analysis situations.
- Data management, including database design, creation, and implementation, documentation, maintenance and quality assurance, and user support for centralized patient and population study databases, including study databases.
- Data analysis for clinical trials and for epidemiologic, cancer prevention and control, and basic science studies.
The best way for eligible faculty to contact the Core is through the walk-in clinics, or by emailing LCCC_BIOS@med.unc.edu.
The UNC Center for AIDS Research (CFAR) biostatistics training core has developed several excellent introductory presentations on statistical concepts relevant to clinical and translational research: Overview of Biostatistics (by Michael Hudgens and Katie Mollan), Data Management (by Ali Fokar), and Survey Development (by Carol Golin and Catherine Grodonsky).
The Department of Pediatrics will be acquiring the Kids’ Inpatient Database (KID) from the Agency for Healthcare Research and Quality (AHRQ) for the use of faculty and fellows who are interested in conducting health services research in large administrative databases – or who wish to learn about using such databases!
The KID is one of the Healthcare Cost and Utilization Project (HCUP) family of databases created and supported by AHRQ. HCUP has been the means of providing researchers with publicly available data at the encounter level. KID contains inpatient treatment and charge data on patients younger than 21 years of age. It is the only all-payer database on children’s health service use.
KID data are captured every three years, and our department will acquire the entire current archive of data from 1997 through 2009. Because the database is large, it permits analysis of rare conditions, but it is also a valuable tool for study of preventable hospitalizations, costs as represented by charges, quality, safety, and comorbidities among other researchable questions.
This link will take you to AHRQ’s KID home page, where you will find considerable information on the contents of the data, and rules for its use.
Several members of the Department of Pediatrics faculty can assist faculty with the use of the data for exploration of research questions. Use of the data does not require a programmer, but some statistical and data analysis experience is helpful. The Department provides some biostatistical support as part of its faculty development portfolio.
Please contact Sue Tolleson-Rinehart for additional information or if you intend to use KID for research projects.