FREE LIVE WEBINAR

July 17, 2025 | 12:00 - 1:00 PM ET

Compassion and compliance in the conduct of clinical research

As clinical research professionals, we are often two-to-three degrees of separation from the research subject upon whose lives much of our work holds influence. However, from conception and ideation, to regulatory reviews and approvals, through execution of a clinical trial, our decisions and leadership impact trial participants and those with direct relationships with research subjects. Empathic considerations for clinical research professionals influence the ethics of clinical research, the practicalities of subject recruitment and attrition, leadership among teams working in high stress environments, and the pursuit of scientific integrity and compliance.

In this webinar, we will discuss the appropriate ways in which empathy and compassion for the populations we work with should be considered in the design of clinical trials, in our interactions with regulators reviewing our research, and importantly in our interactions with study team members who have direct relationships with study subjects.

We'll cover:

• Learn how compassion for research staff and participants can improve trial design, from eligibility criteria to follow-up procedures.
• Explore how empathetic approaches can enhance recruitment, retention, and participant experience.
• Discover MedTech tools that lower trial costs, improve data quality, and streamline PMCF integration.