In this episode, SCRS takes a deep dive into some of the most pressing challenges that clinical trial sites are confronting in 2025. Join us as we explore the current state of site payments, workforce trends, diverse recruitment, and the growing role of technology-enabled trials. We’ll unpack the reasons behind these challenges, from payment terms and reimbursement struggles to the complexities of diversity and technology adoption. Tune in as we discuss how to break through these barriers and create a more inclusive, sustainable and innovative future for clinical trials.

Join Jena Daniels, VP of Customer Value at Medable, as she shares how Medable is transforming clinical trials through patient-centric innovation. Jena shares insights on the value of Medable's Patient Caregiver Network, strategic partnerships with organizations like Rare Patient Voice, and their commitment to supporting research sites.

Tune in to learn how Medable is improving the clinical trial experience for patients, caregivers, and sites alike by incorporating patient and site feedback into their products.

Learn how mobile research units and personalized transportation are transforming access for rural and underserved communities with Dr. Jyoti Angal, Director of Clinical Research at Avera Research Institute (ARI). Dr. Angal discusses the power of intentional recruitment and community outreach to foster inclusion and trust in clinical trials, earning them the 2024 SCRS Excellence in Patient Inclusion Award.  Don't miss expert advice on making clinical research more inclusive and engaging, with strategies to elevate your site's patient recruitment and retention efforts.

In this episode of SCRS Talks, we welcome Rob Hummel, COO and co-founder of Suvoda, to discuss Suvoda’s new role as an SCRS Global Impact Partner. Rob shares insights into Suvoda’s mission to simplify clinical trials for sites and patients through cutting-edge technology. He highlights how Suvoda’s unified platform — featuring core products like eConsent, IRT, eCOA, and ePatient — helps drive greater efficiencies at sites. Rob also offers a look into how artificial intelligence is shaping the future by reducing administrative burdens and allowing sites to focus more on patient care.

Alyssa Boschen, Regional Site Director at IMA Clinical Research, discusses the growing challenge of investigator shortages and how it impacts clinical research studies. Alyssa highlights how advanced practice providers (APPs), such as physician assistants and nurse practitioners, are stepping in to help bridge the gap as investigators. Discover how these medical professionals support research site operations and find new career opportunities in clinical research.

Join Dustin Owen, CEO of Elixia, as he discusses the company's unique Clinical Site Organization (CSO) model and its role in successful clinical trials. With a focus on enhancing patient recruitment and delivering quality data, Elixia is reshaping how trials are managed in complex therapeutic areas like nephrology and psychiatry. Discover their innovative strategies for boosting trial efficiency and overcoming common enrollment challenges with agile site management.

According to the Center for Information and Study on Clinical Research Participation (CISCRP), traveling to a clinical study is the top reason trial participation is disruptive for patients. Learn more about the complexities of patient travel in clinical trials and what the industry is doing about it with Chris Benevides, Director of Patient Travel Services at Elligo Health Research®. Chris offers valuable insights on early planning, risk mitigation, and specialized travel services that can set up sites for success. Discover how travel support can improve patient recruitment and retention, making clinical trials more diverse, accessible, and patient-friendly. 

Discover how patient-finding technology is revolutionizing the way sites identify eligible patients for research studies, streamlining manual processes, and unlocking the potential of electronic health records. Stephen Jasperse from IQVIA and Michal Janota from St. Anne's University Hospital discuss the challenges and breakthroughs with implementing this innovative solution. Explore the benefits of utilizing patient finder technology beyond patient recruitment, including data insights, research support, and improved patient outcomes.

In this episode, Dr. Christine Senn, Senior Vice President of Site/Sponsor Innovation at Advarra, explores the challenges of study startup and the risks posed by working in isolation. She emphasizes the power of moving from siloed processes to integrated collaborations between sponsors, CROs, and sites. Through real-world examples, Dr. Senn demonstrates how this collaborative approach is driving results in healthcare — accelerating timelines, reducing costs, and ultimately improving patient access to clinical trials.

Rare disease trials come with unique challenges, and independent research sites are well-equipped to tackle them. Hamish Baird and Jennifer Botte of Remington-Davis discuss the role of independent sites in rare disease trials and their logistical and operational challenges when executing complex studies. Tune in to hear about effective strategies for patient recruitment, site-sponsor collaboration, and the benefits of flexible, patient-focused approaches in rare disease research.