Archive Available until April 24, 2019
In today’s environment of increasing regulatory compliance, decreasing economics, and growing competition, investigative sites are faced with greater and more complex site management objectives that impact the study budget. Often sites are being asked to assume more and more tasks without adequate remuneration. As a result, sites are generating modest to no operating profits as they absorb these “hidden costs” of conducting and providing quality research. This presentation is being offered as a preview of a 5-part series that SCRS will give in winter 2018.
This presentation will present a pricing case study on a per-subject budget presented to a site, and the challenges that sites face when using that budget to cover all of the costs of conducting that trial. Learning Opportunities
Case studies enhance participants’ understanding and application of the new knowledge they gain.
Tools and techniques will be provided to immediately and dramatically enhance your budgeting process.
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Archive available until May 29, 2019
In this webinar you will learn the practical applications of the blockchain distributed ledger technology and how it is playing a part in delivering real-time access to educational and protocol standards of care. In addition, you will learn how blockchain technology will affect not only the healthcare and clinical research industry as a whole, but how it will affect all healthcare professionals including investigators, nurses, raters, study coordinators, project managers, patients and more.
This presentation will present a pricing case study on a per-subject budget presented to a site, and the challenges that sites face when using that budget to cover all of the costs of conducting that trial. Learning Opportunities
Case studies enhance participants’ understanding and application of the new knowledge they gain.
Tools and techniques will be provided to immediately and dramatically enhance your budgeting process.
learn more...
Archive Available until June 26, 2019
The transition from paper to paperless is an ongoing initiative and a significant challenge within our industry. With challenges that include FDA requirement for Part-11 compliance, sponsor’s reluctance to give control to sites for paperless systems, process development, and communication between sites and other players in the study execution process, there has been a slow uptake of paperless alternatives and processes.
These realities are beginning to change. The benefits of site-based systems are being realized and FDA guidance is being met. However, challenges still remain. Learn what is needed to truly streamline the process for all parties to save time and money, improve accuracy, and speed up the clinical trial process to bring drugs to market faster.
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Archive available until Dec 21, 2019
With the number and complexity of clinical trials increasing significantly, the percent of the clinical research workforce that is disengaged is significant. Coordinators are overburdened and sites cannot afford high turnover. There is a massive talent shortage within the clinical research field and sites are struggling to hire smart and improve performance. Sites can identify the right talent and keep them through better hiring skills and a strong supportive culture. The outcome of a good hire and site culture is higher profitability and productivity, which every site can use in this challenging research market.
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Archive available until May 15, 2019
Attendees will learn how to improve the patient experience during a clinical trial;
Polling questions will be used to ask the audience how patient-centric they feel they are in their current approaches to ensure interactivity during the webinar;
The panel will be comprised of sponsors, CROs and patients to ensure thought-provoking discussion that challenges participants to think differently about the patient journey and our approach.
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Archive Available until June 12, 2019
How do successful sites identify appropriate study opportunities to grow and sustain their clinical trial business? This webinar will share specific methods and essential information required to find new study opportunities, successfully market your site, and create an effective business development plan. Explore how to build and maintain trust and confidence in your relationship with a sponsor/CRO to earn repeat business.
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Archive available until June 19, 2019
The digital era is upon us and here to stay, and it comes as no surprise that the future of effective patient recruitment lies online. During this webinar, the audience will learn how to effectively develop and implement a multi-platform digital marketing strategy identify, recruit, enroll, engage and retain clinical trial subjects. We will discuss new, innovative digital marketing tools and tactics (i.e. Facebook, Twitter, Google Analytics, study website, etc.) to help boost clinical trial recruitment and retention. We will also explore the necessary steps for building and optimizing components of your study website. Take advantage of this opportunity to learn how to successfully expedite the recruitment process and enhance a patient’s overall experience.
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Archive available until July 10, 2019
The value of your site is in the eye of the prospective buyer; therefore, site owners should position their businesses to drive the strategic value and attractiveness before a possible sale transaction. With numerous complexities surrounding the sale of your site, early implementation of an exit strategy will enhance the value of your business, minimize “surprises” throughout the transaction process, and lead to a successful transaction.
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Archive available until July 17, 2019
Is your site eConsent ready? As more study sponsors prefer to work with sites that are familiar and engaged with electronic informed consent (eIC) forms and solutions, this webinar will focus on best practices that ensure compliance and operational efficiencies. Find out how to prepare your site to be ready regardless of the eConsent solution or vendor.
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Archive available until July 24, 2019
While still highly fragmented, the consolidation that continues to impact the CRO industry has started to flow down to the clinical trials site sector. Barry Lake, CEO of Devana Solutions®, will provide insights into timing and performance metrics data that sites can leverage to position themselves as sector leaders and enhance valuation for a successful exit sale.
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Archive Available until March 5, 2020
Understanding the ins and outs of research billing compliance and research billing regulations can be a difficult task, but with the proper knowledge of these subjects, researchers can successfully apply appropriate billing practices.
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Archive Available until March 26, 2020
Join this webinar to learn the primary tools and best practices utilized by hospital-based research sites that will empower your team members to utilize consistent, clear and effective communication strategies.
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Archive Available until March 28, 2020
Join PAREXEL for a discussion on contracting and budgeting in Poland.
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