Expert highlights how clinical research professionals can and should “form partnerships with grassroots organizations that would build trust between us and the community.”
“Certification is indeed valuable, and we must expand education and training in the domains that our survey found might be lacking.”
Patient recruitment is “not just about finding ways to talk to the patients already in our database,” thought leader warns.
“There’s lots you can do even before the clinical trial starts to be more inclusive of the LGBTQ+ population.”
Sponsors who turn to the same study sites over and over again are missing out on others with sturdy local roots in underserved communities, expert says.