Category Archive: Child of Community

Partnerships


We understand the importance of working with the local community to share and disseminate clinical research findings.   We strive to build and maintain relationships with those that have a common goal. This is a working list of current and potential Johns Hopkins University community partners in Baltimore City, inclusive of student, staff and faculty participation in programs or organizations.   HopkinsLocal Website

The Henrietta Lacks Memorial Lecture


The goal of the series is to honor Henrietta Lacks and the positive global impact of HeLa cells. This series will also serve as an annual reminder of the gratitude, respect, and clear communication due to all research participants. Keeping biomedical research connected to the people it is intended to serve is an ongoing process rooted in the open exchange of ideas among all stakeholders. To facilitate this process, speakers for the Henrietta Lacks Memorial Lecture Series are selected for their ability to communicate the current ethical complexities and challenges facing biomedical research in a way that is engaging and […]

Research Participant Advocate


The Research Participant Advocacy Program offers consulting expertise on human subjects and regulatory issues, IRB applications, the informed consent process, study feasibility and good clinical practice (GCP). Our advocates serve as a resource to research teams and research participants by reviewing applications to the Clinical Research Unit to assure high standards for human subjects protections. Contact our team to review consent forms, protocol or data and safety monitoring plans. The Research Participant Advocate is available to participants or potential participants to address issues or complaints relating to research participation. They can also answer questions you  may have about research in […]

MyChart Recruitment Messages


Johns Hopkins Medicine is committed to supporting the discovery of new ways to improve the care and outcomes for patients.   Patients throughout the Johns Hopkins Health System have access to a network of clinical research studies for many different conditions. In November 2016, the Johns Hopkins Research Participant Recruitment and Retention Program piloted a program to inform patients of research studies through automated MyChart Recruitment Messages. Our goal is to empower patients by connecting them with clinical research studies that may be of interest to them. In a recent survey, we assessed what patients think about MyChart research invitations; […]

Community Research Advisory Council (C-RAC)


The Community Research Advisory Council creates a forum for patients and diverse stakeholders to help shape research conducted at Johns Hopkins.