Our Voice | Our CommunityYour Success

The Society for Clinical Research Sites (SCRS) was founded in 2012 in response to the growing need for a global organization representative of the needs of clinical research sites globally. SCRS currently represents over 9,500 research sites in 47 countries. SCRS’ mission is to unify the voice of the global clinical research site community for site sustainability. SCRS is an active partner in industry-wide initiatives and dialogues focused on improving the clinical research enterprise.

TESTIMONIALS

Great conference.  Very substantive, speakers were willing to share real information – not just skimming the surface.  Attendees seemed eager to network and talk.
Molly G. HugginsPartnerHuggins & Zuiker, LLP

UPCOMING WEBINARS

Oncology Clinical Trials: A Necessary Dialogue Between Patient, Site and Sponsor
April 6, 2021 (12:00 pm ET)

Virtual Study Training from the Sponsor and Site Perspectives
April 13, 2021 (12:00 pm ET)

How Can We Be More Inclusive to Minorities in Clinical Research - The Site and Patient Voice Matters!
April 15, 2021 (12:00 pm ET)

Reimagining Feasibility: From Transaction to Partnership
April 27, 2021 (12:00 pm ET)

TWITTER @MYSCRS

Thank you to our April SitesNOW supporters & panelists, Ken Getz of @CISCRP,@TuftsCSDD & Casey Orvin of @Studykik. Today's discussion was all about sharing ideas & channels for patient engagement & patient recruitment.

Register for the next discussion: https://t.co/eDzxKdMPqn

Join us for a webinar on April 13 at 12PM ET on how virtual training and site engagement tools are evolving and can facilitate trial conduct, enhance Site performance, and yield improved outcomes from the Sponsor and Site perspective. Register: https://t.co/PoSeQOIsXd

We strongly support diversity in #ClinicalTrials! Our President @karrivenn will be speaking at @MySCRS' webinar on Thursday, April 15, 2021, to cover @LMCManna's advisory patient committee model with a special focus on #diversity ✨Join us!

Register: https://t.co/YupxeiPSNT

At @MySCRS, European Site Solutions Summit, @Medidata's Fiona Maini will join a panel discussion on what rSDV/rSDR looks like now, how it can help the transformation to remote #clinicaltrials + how tech companies work together to mitigate site burden: https://t.co/R9Mit8Tx19

How can we improve as an industry to encourage accountability and sustainability of diversity, equity, and inclusion in drug development?

Join the discussion at the virtual meeting with @DrugInfoAssn on April 27: https://t.co/BTs3gr41Jl

New survey opportunity by @TuftsCSDD to better understand diversity and disparities among staff at clinical research sites around the world. Participate here: https://t.co/zm9guPpI1y

Kits4Life recently launched to address the amount of waste produced by unused trial supplies by donating them to humanitarian aid organizations in 90+ countries. Learn how you can get involved: https://t.co/vFP2r54dhN

We are 2 weeks away from @MySCRS European Site Solutions Summit! Join us for this virtual conference as we cover the future of sites at the plenary session. Learn more and register today: https://t.co/2LJQf6o7CW #SCRS21Europe

In this #whitepaper, Medidata partnered with @MySCRS to measure sites' current & anticipated levels of adoption or patient-centric tools, and the sites' perspective on how #patients have reacted to them. Download your copy here: https://t.co/jUizBJbXmp

The Spring 2021 issue of the SCRS InSite Journal is live! Learn how sites can maintain quality assurance through the pandemic, considerations for implementing new technology into your clinical trials, the new SCRS Diversity Program, and more: https://t.co/BWOJ2ARS8a

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