In addition to and in-person and virtual Patient Advisory Boards and Patient Clinical Trial Journey Workshops, CISCRP also conducts in-depth interviews, online surveys, and facilitates discussions among cross-functional teams. We work collaboratively with your organization to design a research plan that meets your objectives.

Custom research projects include:

• Assessing volunteer response to new informed consent technology
• Gauging volunteer commitment and satisfaction in a long-term trial
• Testing patient understanding and adherence to a draft protocol
• Evaluating the feasibility of ‘crowdsourcing’ patient input for protocol design
• Gathering volunteer feedback on satisfaction with clinical supplies
• Testing of a new clinical trial application