Meet the HCRN Clinical Research Coordinators

Map of HCRN Centers 2016

Our coordinators bring widespread expertise to the network, with backgrounds in business administration, grant writing, database development, epidemiology, education, and nursing. The coordinators’ responsibilities are diverse and some aspects of their work vary from center to center, but they all work together to achieve the same end: ensuring the highest standards of quality in all HCRN research activities. The research coordinators are actively involved in the preliminary phases of the research studies:

• Research proposal development and budgets

• Study protocol and data collection forms production and editing

• Internal Review Board/Research Ethics Board (IRB/REB) communication and approval process

Once a study is underway the coordinators are the key people involved in daily study activities:

• Meeting with patients and their families to discuss potential participation in HCRN studies

• Collecting and entering study data – often in the operating room during surgery

• Maintaining accurate and confidential records of each participant

• Managing study amendments and ongoing IRB/REB approval

Furthermore, our coordinators ensure the highest quality of data collection and compliance has been achieved as they prepare data for analysis. The coordinators assist with a variety of other tasks, such as gathering information needed for grant applications, serving as liaisons with their institution’s grants and contracts offices, and organizing and hosting HCRN bi-annual meetings which rotate among the various clinical centers.

These are the team members who often work behind the scenes, and without them, we would be unable to conduct the innovative research that is the hallmark of the HCRN.