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© 2024 SCRS Talks
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SCRS Talks, hosted by the Society for Clinical Research Sites (SCRS), is a platform for clinical research industry professionals to hear about valuable information shaping the research industry today. These short interviews will provide new perspectives and insights on pressing topics, current events, and the research community.
163 Episodes
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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 int...
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, ...
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...
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 s...
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, resear...
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 a...
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.
As technology drives breakthroughs in clinical research, it's also transforming how clinical trials are managed. Join Clay Williams, Vice President of Mobile Applications at Greenphire, to learn how their platform GreenSpace is simplifying clinical trial participation. From submitting receipts to tracking reimbursements, hear how GreenSpace removes barriers for both participants and sites, and how it’s impacting projects like the Metastatic Breast Cancer Alliance's patient registry.
Rosie McKellar, CEO of the Pacific Clinical Research Network (PCRN) New Zealand, shares insights from her organization’s innovative network partners model and their deep commitment to patient outcomes. PCRN’s efficient recruitment strategies and speedy trial execution have positioned New Zealand as a key player in global clinical research. Rosie also discusses PCRN’s collaboration with SCRS as a Global Impact Partner and what’s next for clinical research in New Zealand and Australia.
Join us as we welcome new SCRS team member Lauren Stockwell, Content and Engagement Manager, with an insightful conversation about the value of mentorship in the clinical research community. Lauren shares her passion for empowering the next generation of clinical research professionals, highlighting SCRS's newly launched Mentorship Program. Explore how purposeful mentorship can elevate site professionals both personally and professionally, and offer practical tips on how site members can get ...
Leigh Burgess, CEO and founder of Bold Industries Group, reveals how applying design thinking can transform clinical research operations. Learn how radical prioritization and the innovative D90 framework can help organizations cut through complexity, enhance teamwork, and accelerate trial results — delivering more efficient outcomes for patients and stakeholders alike.
Michelle Ray, Director of Customer Success with Greenphire, explores the challenges that delayed payments pose to research site sustainability. Michelle highlights key issues like the burden of delayed payments on site operations and recruitment, the complexity of invoicing, and the role of technology in simplifying payment workflows. Learn how innovating payment systems can streamline financial processes, creating a more sustainable future for sites, patients, and sponsors alike.
Renuka Agarwal, CEO and co-founder of UpTrials, is revolutionizing site workforce challenges. Renuka shares the inspiration behind founding UpTrials, and how the platform is making a significant impact by matching research sites with skilled candidates. Learn how UpTrials is streamlining the hiring process, improving time-to-fill rates, and bringing much-needed innovation to clinical research hiring processes.UpTrials is AI-driven software designed to help clinical research employers hire top...
In this episode, we'll explore the transformative power of collaboration and advocacy in the pursuit of life-altering treatments. Meike Madelung from IQVIA's EMEA Thought Leadership team takes us through a compelling case study featuring the AKU Society and its groundbreaking efforts in combating Alkaptonuria. Learn how patient organizations can help accelerate recruitment for rare disease trials.
Input from research sites is essential for developing clinical technologies that are practical, efficient, user-friendly, and aligned with the real-world needs and challenges of trials. Understanding this need, Medidata Solutions hosted an interactive Site Tech Board through SCRS to learn how to improve their technology and processes directly from sites. Tune in as Robin Douglas, Vice President of Research Site Engagement at Medidata, highlights how the organization is creating a better exper...
Ophthalmology, a medical specialty focusing on the structure, function, and diseases of the eye, has a growing role in non-ophthalmic studies. Jessica Mays, Vice President of Life Sciences at 20/20 Onsite, shares common challenges sites face with trial-related eye assessments and how to accurately budget for these types of services. Tune in to learn how 20/20 Onsite is making ophthalmology research more accessible to sites and patients through mobile services.
Celebrate clinical trial innovation with Catherine Pitman, Lead Research Nurse at University Hospitals Plymouth NHS Trust, recipient of the 2023 European Site Spark award. Catherine shares how the pandemic brought on new opportunities to enable more accessible clinical trials through the launch of a Mobile Research Unit (MRU). Hear how her organization's passion brought on new ideas and resolutions to problems created during the pandemic, and ultimately led to Plymouth Research and Developmen...
Michelle Hartmann, Director and Owner of South Broward Research, speaks with David Unger, Director of Operational Excellence and Site Payment Lead at Merck, about tackling clinical research site payment delays. David shares how Merck identified and addressed key challenges in their payment processes, leading to more timely payments and improved site satisfaction. Hear how Merck implemented various strategies including system upgrades, process simplifications, and better communication with sit...
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