clinical research Service Provider formerly known as a CRO
Reliable Partners in Clinical Research
We specialize in accelerating clinical trials without compromising quality or compliance. Our expert management team combines decades of experience with cutting-edge methodologies to streamline every phase of your clinical research. From protocol development and site selection to data management and regulatory submissions, we ensure your trials progress swiftly and efficiently. Our comprehensive approach mitigates delays, optimizes resources, and delivers reliable results, enabling you to bring innovative therapies to market faster.
We understand that time is critical in clinical research, especially when it comes to life-changing medical advancements. That's why we offer a tailored, responsive approach designed to meet your specific needs and timelines. Our support services extend beyond traditional project management, providing you with strategic insights and operational excellence throughout the trial lifecycle. Partner with us to leverage our proven expertise and robust support infrastructure, and watch your clinical trials move seamlessly from concept to completion, helping you achieve your research goals faster and more effectively.
Site and Sponsor Partners
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Site and Sponsor Partners ✦
Empowering Clinical Research Innovations
We redefine traditional clinical research methodologies by embracing an unconventional, site-centric, and results-driven business model. Our unique approach focuses on synergistically sharing the success of the study experience with patients, sites, vendors, and sponsors. By prioritizing the needs and perspectives of each stakeholder, we foster a collaborative environment that enhances engagement, efficiency, and outcomes. This site-centric strategy ensures that clinical sites receive tailored support and resources, optimizing patient recruitment and retention while reducing administrative burdens. Our commitment to a results-driven philosophy means that we are relentless in our pursuit of high-quality, actionable data, ensuring that each study not only meets but exceeds its objectives. This holistic, integrated approach sets us apart, driving innovation and excellence at every stage of the clinical trial process, and ultimately leading to more effective therapies and better patient outcomes.
Our Contract Research Organization (CRO) was founded by industry veterans renowned for their exemplary reputations and deep-rooted expertise in clinical research. Our founding members have cultivated critical relationships and influence with clinical sites and technology vendors, establishing a robust network that sets us apart from traditional, larger CROs. This unique positioning allows us to offer a more personalized and responsive approach, ensuring that sponsors, who may have felt overlooked or underserved by larger organizations, receive the dedicated attention and customized solutions they deserve. Our trusted relationships with leading sites and cutting-edge technology providers enable us to streamline operations, enhance study efficiency, and deliver superior results. By leveraging these strategic partnerships, we provide an unparalleled level of service, making us the ideal choice for sponsors seeking a CRO that combines innovation, agility, and deep industry connections.
taking responsibility
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taking responsibility ✦
Biography for Robert Goldman
Robert S. Goldman
Co-Founder & COO
Robert S. Goldman brings over 16+ years of unparalleled experience in clinical research and drug development to his role as Co-Founder and COO of neXgenTrials. A seasoned leader and innovator in the industry, Robert is driven by a passion for accelerating medical advancements through efficient and high-quality clinical trials.
Robert’s extensive background includes serving in pivotal roles where he has consistently demonstrated his expertise in clinical operations, project management, and strategic planning. His career spans leadership positions at renowned organizations such as INC Research , PPD, and PRA Health Sciences, where he played a critical role in overseeing global clinical trials, driving operational excellence, and fostering strategic partnerships.
In his previous roles as Head of Clinical Operations, Robert led a team responsible for the successful execution of complex, multi-national clinical studies. His leadership was instrumental in enhancing operational efficiencies and delivering high-quality data, contributing significantly to the development and approval of several key therapies.
Robert was pivotal in managing large-scale, multi-phase clinical trials, where he implemented innovative approaches to project management and site engagement, resulting in improved timelines and deliverables. Robert’s Management showcased his ability to lead cross-functional teams and streamline processes to optimize trial outcomes.
Robert holds a Bachelor’s degree in Medical Technology and clinical laboratory science from Michigan State University, studied at Wayne State University for his Master of Science and attended St. Mathew’s University School of Medicine pursuing his MD. He has pursued advanced training in clinical research management and leadership. His commitment to professional development is reflected in his continuous efforts to stay abreast of industry trends and advancements.
A thought leader in the clinical research community, Robert frequently contributes to industry conferences and publications, sharing insights on topics such as patient recruitment, site management, and technological innovations in clinical trials.
At neXgenTrials, Robert’s vision is to create a site-centric, results-driven CRO that delivers superior value through collaboration and innovation. His reputation for building strong relationships with clinical sites and technology vendors underscores his ability to drive success in clinical trials, making him a trusted partner for sponsors seeking a more personalized and effective approach to their research needs.
MEET the founders
Biography for Chris Sauber
Chris Sauber
Co-Founder & CFO
Chris Sauber, Co-Founder and Chief Financial Officer of neXgenTrials, is a dynamic leader with a profound impact on the clinical research industry. With over a decade of hands-on experience and a passion for site-centric innovation, Chris has become a recognized expert in optimizing clinical trial operations and site management.
As the driving force behind DSCS Clinical Research, a prominent consulting firm specializing in clinical trial solutions, Chris has demonstrated an exceptional ability to enhance site efficiency and foster strong relationships between clinical sites and sponsors. His work at DSCS has been pivotal in addressing the operational challenges faced by clinical research sites, providing them with tailored solutions that streamline processes and improve overall study outcomes.
Chris is also the founder of Save Our Sites, an influential initiative dedicated to supporting clinical research sites through educational resources, advocacy, and strategic guidance. Under his leadership, Save Our Sites has become a vital resource for sites navigating the complexities of clinical trials, empowering them with the knowledge and tools necessary to thrive in an ever-evolving landscape.
In addition to his entrepreneurial ventures, Chris co-founded Latinos in Clinical Research, an organization dedicated to increasing diversity and inclusion within the clinical research industry. Latinos in Clinical Research provides networking, educational, and professional development opportunities for Latino professionals and aims to address the underrepresentation of Latinos in clinical trials. The organization has quickly become a leading advocate for promoting diversity and supporting Latino professionals across the clinical research spectrum.
Chris is also a co-author of The Comprehensive Guide to Clinical Research, a widely acclaimed resource that serves as a cornerstone for professionals seeking to understand the intricacies of clinical research. The guide is renowned for its practical insights and actionable strategies, reflecting Chris's deep understanding of the field and his commitment to advancing clinical research practices.
Chris also owns and operates clinical sites and has negotiated and managed thousands of site contracts and budgets over the years through his consulting firm. Widely regarded as one of the industry’s leading experts in budget negotiation from the clinical site perspective, Chris brings a wealth of experience and proficiency to ensuring favorable terms and efficient management for site operations.
At neXgenTrials, Chris's innovative vision and operational acumen drive the organization’s commitment to delivering exceptional clinical research services. His dedication to fostering site-centric solutions and building robust, supportive relationships with clinical sites and sponsors underscores his role as a key player in transforming clinical trial operations. Chris’s strategic insights and collaborative approach make him an invaluable asset to the organization and a trusted partner for clients seeking a CRO that prioritizes efficiency, engagement, and excellence.
Biography for Dan Sfera
Dan Sfera
Co-Founder & CEO
Dan Sfera, Co-Founder and Chief Strategy Officer of neXgenTrials, is a visionary leader and influential figure in the clinical research industry. With a career spanning over 15 years, Dan has dedicated himself to advancing clinical trial practices through innovative strategies, extensive knowledge sharing, and a commitment to site-centric solutions.
Dan is the driving force behind The Clinical Trials Guru, a leading resource for clinical research professionals. As the founder, he provides valuable insights, educational content, and practical advice on navigating the complexities of clinical trials. Through his engaging blog posts, webinars, and in-depth articles, Dan has become a trusted source of information for both newcomers and seasoned professionals in the industry.
In addition to his work with The Clinical Trials Guru, Dan is a prolific content creator and educator through his YouTube channel. His channel features hundreds of videos covering a wide range of topics related to clinical research, including patient recruitment, site management, regulatory affairs, and career development. Dan’s ability to break down complex topics into accessible, actionable content has earned him a loyal following and recognition as a leading voice in clinical research education.
Dan also brings a wealth of hands-on experience from his role as a Site Owner at Yuma Clinical Trials and Consultant at DSCS Sweat Equity & Investments. He has successfully managed multiple clinical trial sites, where he has honed his skills in site operations, patient engagement, and study execution. His consulting work includes providing strategic guidance to clinical research sites and sponsors, helping them optimize their trial processes and achieve their research objectives.
Furthermore, Dan is the co-author of The Comprehensive Guide to Clinical Research, a definitive resource that offers an in-depth exploration of clinical research methodologies and best practices. The guide reflects Dan's deep understanding of the industry and his commitment to elevating the standards of clinical research through education and strategic insight.
At neXgenTrials, Dan leverages his strategic acumen and industry expertise to drive the organization’s growth and success. His dedication to fostering site-centric strategies and enhancing the clinical trial experience for all stakeholders underscores his role as a key architect of the company’s strategic vision. Dan’s influence and thought leadership make him a valuable asset to the organization and a trusted partner for clients seeking a forward-thinking and effective approach to clinical research.
STRATEGIC SERVICE PROVIDER
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STRATEGIC SERVICE PROVIDER ✦
SERvices
We offer comprehensive, full-service support for your clinical research needs, with a particular emphasis on site selection, mentoring, and enhancing patient accrual. Our approach to site selection is meticulous and data-driven, ensuring that we identify and engage the most suitable clinical sites for your studies. We leverage our extensive network and industry insights to select sites that not only meet the operational and regulatory requirements but also have a proven track record in patient recruitment and retention. This strategic site selection process minimizes start-up delays and maximizes the potential for successful trial outcomes.
In addition to site selection, we provide robust mentoring programs designed to support and elevate clinical sites throughout the trial lifecycle. Our mentoring services include personalized training, operational support, and ongoing guidance tailored to the specific needs of each site. We work closely with site staff to enhance their capabilities, streamline processes, and address any challenges they may encounter. This hands-on mentoring ensures that sites are well-prepared and equipped to handle the complexities of clinical trials, ultimately leading to more efficient operations and higher quality data.
Furthermore, we recognize that effective patient accrual is critical to the success of any clinical trial. Our organization excels in implementing strategies that drive patient engagement and improve accrual rates. We utilize a combination of traditional outreach and innovative digital tools to identify and recruit eligible participants, ensuring a diverse and representative patient population. Our influence in the industry, combined with our site-centric approach, enables us to foster strong relationships with sites and communities, facilitating smoother and faster patient recruitment. By integrating these elements, [Your Contract Research Organization Name] ensures that your clinical trials are not only conducted efficiently but also yield meaningful, high-quality results.
NO OBLIGATION CONSULTATION
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NO OBLIGATION CONSULTATION ✦
