Industry partnerships enhance the flow of communication between clinical trial stakeholders and increase connection to crucial resources. As we strive daily for improved access to and diversity within clinical research, working together strengthens our community and allows us to reach a broader audience. In these mutually-beneficial agreements, each stakeholder has an active interest in the other and strives to reach collaborative success. Additionally, future industry partnerships will lead to a systematic approach that could revolutionize our industry in the future.
The Center for Information and Study on Clinical Research Participation’s (CISCRP) core mission is to provide accessible, relevant, useful, high-quality educational resources, programs, and services to:
ClinEco is a web-based platform and community connecting the stakeholders of conventional, decentralized, and hybrid clinical trials.
The ClinEco platform and marketplace enable accelerated identification of high-value providers and partners.
Clinical Trials For All is a nonprofit educational initiative designed to inform the public about clinical research with the goal of making patient participation diverse, equitable, and widespread.
Greater Gift is an independent, 501(c)(3) nonprofit founded in 2010 to increase clinical research awareness, build trust through the celebration and expression of gratitude for everyone involved in clinical research, and pay forward the gift of health created by the participants and all contributors to clinical research. Over 160,000 clinical trial participants and contributors are recognized for their contributions to clinical research and world health.
Dedicated to expressing gratitude and paying it forward, we help children in need of vaccines and support those facing food insecurities.
Additionally, we empower minority students by funding, through donations, a scholarship program, fostering a diverse workforce for the future of clinical research, and providing students an opportunity to pursue their dreams.
Karen’s Club connects cancer patients of color with life-saving treatments. People of color continue to experience medical bias and lack of access to quality healthcare. Karen’s Club is uniquely tackling the distrust and information barriers to make a meaningful impact and be a valuable resource to the community.
The National PKU Alliance (NPKUA) is a collaboration of PKU community members joining together as a national voice and supporting local efforts to raise PKU awareness and drive advocacy and education while ultimately looking for a cure.
The National Organization for Rare Disorders (NORD) advances practical, meaningful, and enduring change so people with rare diseases can live their fullest and best lives. For 40 years, we have worked every day to elevate care, advance research, and drive policy in a purposeful and holistic manner to lift up the rare disease community.
Rare Patient Voice(RPV) connects patients and family caregivers of rare and non-rare diseases with opportunities to share their opinions with companies and researchers by participating in all types of research studies. These include surveys and phone interviews, online bulletin boards, focus groups, clinical trials, and more.
While RPV began with a focus on rare diseases, we now welcome patients and family caregivers living with all medical conditions. We currently cover over 1,400 rare and non-rare diseases and conditions.
SiteBridge Research is a research organization connecting physicians with clinical trial opportunities, so they can offer those opportunities as a healthcare option to their patients. We aim to improve community health outcomes, especially those of racial/ethnic minorities and underrepresented populations, through clinical trial participation.
Bridging the Gap in Clinical Trials Arts Contest 2023 – Social Media Champion
Beginning June 15, adults ages 18 and older can submit entries to the contest’s four categories: visual arts, music, photography, and dance.
Those interested in participating must adhere to one of four different themes: personal experience, improved health outcomes, impact on family, friends, or community, and access to medicine.
Individual awards range from $500-$2,000 and winners will be notified in November 2023.
Women’s Cancer Research Network (WCRN) brings cutting-edge clinical trial enrollment opportunities to underserved communities and local clinics.
Our mission at WCRN is to help bring new and innovative clinical trials to women with breast and gynecological cancers in partnership with sponsor companies and clinics to help end cancer.
Clincierge is proud to support CISCRP in a new educational initiative to increase awareness about clinical research and the level of understanding among minority communities across the U S We have united to circulate an informative full page advertorial spread highlighting the key importance of diversity in clinical studies to
Each February the rare disease community celebrates Rare Disease Month Started in 2008 by the European Organization for Rare Diseases EURORDIS the event brings together rare disease patients caregivers and advocacy organizations across the globe to advance awareness and increase research opportunities The Rare Disease Month celebration culminates in Rare
Clincierge is proud to support CISCRP in a new educational initiative to increase awareness about clinical research and the level of understanding among minority communities across the U S We have united to circulate an informative full page advertorial spread highlighting the key importance of diversity in clinical studies to
Learn more about partnering with Clincierge
