Biomedical Researcher Resources: Duke Resources

A guide for researchers who are trying to learn about and implement community engagement in their work.

A List of the 30+ state-of-the-art shared research facilities that are available for use by all Duke investigators.

Tailored guidance on My Research Path for those new to Duke or new to research on navigating the processes, requirements, and resources associated with scholarly research at Duke.

Duke's Research Policy Manual compiles the University’s current research policies into a single, well organized, searchable volume so all individuals in the Duke research community can know and apply the institutional expectations and best practices for conducting research at Duke.

Research Toolkits is a self-service portal for researchers to get access to and manage their research computing services including managing access to project-based virtual machines with storage and to the Duke Compute Cluster (DCC).

Courses on data management and quality as well as research communication and data dissemination provided by ASIST. May be taken for RCR-100 online credit.

Duke's participation in several Clinical Data Research Networks (CDRNs) makes it easier to conduct multi-site studies by enabling access to well-curated EHR data at all member institutions, including Duke.

The BERD Methods Core helps investigators find methodologists for collaboration (e.g., biostatisticians, data scientists, qualitative scientists, epidemiologists)

Collaborative effort to provide a one-stop shop for Duke investigators to learn about and access a wealth of data resources.

The CRU will provide infrastructure, resources, and support to help Duke investigators, from any school at Duke University, translate ideas into innovations that improve health.

Through CDVS, get support for research data management, data visualization, mapping and GIS, and more.

Information and resources for using animals in research and education at Duke.

DOCR assists with various functions through all study phases, including billing risks, patient billing, clinical research training, and policies for the review and approval of projects.

Responsible for supporting investigators and administrators in the SOM and SON by managing externally sponsored research projects through the pre-award process.

Oversees: The Grants, Contracts, & Compliance group; The Funding Opportunities group; The Office of Human Subjects Protection; The Office of Export Controls

The OSP safeguards project funds, maximizes the University's cash flow position, and maintains good relations with sponsoring agencies and University personnel.

The primary resource for financial research compliance management, providing oversight and guidance to the research community in the management of sponsored projects funding.

The Duke University Compliance Program provides oversight for compliance activities in three areas: Human Subject Research Compliance, HIPAA/Privacy, and Compliance Monitoring.

Provides comprehensive trial support services, led by faculty, biostatisticians and operational teams.

DCRI partners with digital health innovators to bring clinical insights to groundbreaking applications that improve health outcomes. Capabilities include: study design, regulatory planning, protocol development,data analysis, comparable effectiveness studies, feasibility studies, real-world data studies, RCTs.

Offers cutting-edge imaging interpretations for all phases of clinical trials.

A solution for incorporating pharmacogenomic studies into clinical trials, providing sponsors with an “insurance option” to quickly investigate genetic association with adverse events or efficacy after clinical trial completion.