— Archives - Society for Clinical Research Sites – SCRS
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Join SCRS President, Christine Pierre, for an in-depth interview with industry leaders.Continue reading…

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E-patients are a staple in the healthcare landscape. Their powerful influence is well-known as an accelerator for the discovery of treatments and cures. During this workshop, attendees will uncover the role of the e-patient and learn how to incorporate their voice into clinical research sites.Continue reading…

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As our industry continues to evolve, the “Patient’s Voice” has become a more recognizable and integral part of the clinical development process.Continue reading…

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This educational webinar will help investigative sites prepare for the potentially disruptive shift toward greater use of mobile technology to capture objective data in clinical trials.Continue reading…

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As protocols become increasingly complex, many sites struggle to keep up with all the requirements of managing studies, let alone a business. By using electronic source, sites can drastically increase efficiency by eliminating redundant tasks, enabling remote collaboration and improving data quality at the point of capture. This session will clarify the PI’s right to utilize eSource and provide a case study on the productivity benefits one site that went paperless experienced. It will discuss how source data capture is more accurate and streamlined than with paper when utilizing an appropriately designed technology.Continue reading…

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This webinar reviews the updates to the International Conference for Harmonization (ICH) Good Clinical Practice (GCP) E-6 Guideline published in 2016. As research sites conduct clinical trials for sponsor and other organizations, it is critical for sites to understand the changes to this protocol required GCP that sites are expected to follow for their clinical trials. Register for this webinar for a high-level overview of the changes and clinical research practices impacted by the new requirements that serve as a starting point for an organization’s internal review and GCP compliance.Continue reading…

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As protocols become increasingly complex, many sites struggle to keep up with all the requirements of managing studies, let alone a business. By using electronic source, sites can drastically increase efficiency by eliminating redundant tasks, enabling remote collaboration and improving data quality at the point of capture. This session will clarify the PI’s right to utilize eSource and provide a case study on the productivity benefits one site that went paperless experienced. It will discuss how source data capture is more accurate and streamlined than with paper when utilizing an appropriately designed technology.Continue reading…

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In today’s environment of increased regulatory compliance, decreasing economics, and growing competition, investigative sites are faced with greater and more complex site management objectives. Often sites are being asked to assume more and more tasks without adequate remuneration.Continue reading…

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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.Continue reading…

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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.Continue reading…

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Small sites often have bottom lines that don’t allow for expensive and redundant training for their research staff. In this discussion you will learn about the general industry training requirements, and frugal resources to utilize when training your staff. Best practices will be shared to support sites in providing high-quality training at a reasonable cost.Continue reading…

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In this webinar you will learn how to think differently and strategically to ensure your site remains front and center in clinical site operations, recruitment and compliance. Key items discussed will include business development, centralized services, patient engagement, and risk-based quality management from the site perspective.Continue reading…

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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.Continue reading…

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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.Continue reading…

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Is your site eConsent ready? As more study sponsors prefer to work with sites that are ready to consent with electronic informed consent (eIC) forms and solutions, this webinar will focus on best practices that ensure compliance and operational inefficiencies. Find out how to prepare your site to be ready regardless of the eConsent solution or vendor.Continue reading…

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Join SCRS President, Christine Pierre, for an in-depth interview with industry leaders.Continue reading…

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Join PharmaSeek and SCRS for a discussion on behavioral economics and learn to identify cognitive biases that could be influencing your clinical trial negotiations.Continue reading…

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Whether your site plans to grow organically or with a strategic plan, your goal is to build a high performing team to do quality work for your sponsors, CROs, and most importantly, your patients. In this webinar, we will discuss key factors to determine before building your team, define qualities to look for (and screen out) in the interview process, and then the process of building your team starting from a small to a large site.Continue reading…

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Digital media is all the rage – but that doesn’t mean it’s the ONLY way to advertise. When thinking about your advertising budget, it is best to diversify your funds across a variety of both traditional and digital mediums to gain the most reach. Join PatientWise for a webinar on “New Year’s Resolution: Diversify Your Recruitment Funds” to learn more about utilizing your advertising dollars to the fullest amount.Continue reading…

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How do successful sites identify new study opportunities to sustain and grow their clinical trial business?Continue reading…

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Few study sites have transitioned to an electronic Regulatory Binder system because they’re perceived to be time-consuming, complicated and risky. New technology has lowered the hurdles and streamlined the study site’s transition to going electronic. This webinar will describe the overwhelming benefits of moving to electronic binders and will show how to make the transformation seamless and reliable.Continue reading…

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Sites are regularly provided with technology from sponsors and CROs that are supposed to make running trials easier and faster. Yet many sites struggle with the plethora of portals, training sessions, passwords, and hardware needed to run the technologies.Continue reading…

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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.Continue reading…

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Few study sites have transitioned to an electronic Regulatory Binder system because they’re perceived as being time-consuming, complicated and risky. New technology has lowered the hurdles and streamlined the study site’s transition to going electronic. This webinar will describe the overwhelming benefits of moving to electronic binders and will show how to make the transformation seamless and reliable.Continue reading…

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Few study sites have transitioned to an electronic Regulatory Binder system because they’re perceived as being time-consuming, complicated and risky. New technology has lowered the hurdles and streamlined the study site’s transition to going electronic. This webinar will describe the overwhelming benefits of moving to electronic binders and will show how to make the transformation seamless and reliable.Continue reading…

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Understand the risk and exposures that sites face when performing clinical trials. Insurance is one tool to transfer risk but aligning contractual obligations and insurance is vital to protect your organization. We will go over the nuances of an ideal insurance policy and discuss the critical areas of a contract to be aware of.Continue reading…

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Ask any clinical research professional what CAPA is and you will likely get a wide variety of responses and interpretations. This creates untold confusion in our industry and leaves many equating CAPA with a negative connotation. In this session we will break down what CAPA is all about.Continue reading…

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Many clinical research sites are looking to improve efficiency and reduce the burden of paper.Continue reading…

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Learn how participant stipends, travel and reimbursements are a critical factor to patient access and retention. Hear first-hand from sites who have implemented an automated approach and the dramatic ROI it has produced.Continue reading…

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While we know that patient recruitment continues to be a challenge across the drug development industry, perhaps one of the greatest challenges is being able to actively engage and retain enrolled patients throughout the life of the trial. In this webinar, IQVIA’s Marie Lux, senior director, Site and Patient Networks and Kimberly Powers, Director, Site and Patient Networks will share best practices for retaining patients including patient-centric tools and strategies.Continue reading…

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Indemnification language is contract language that can provide your site with a benefit or a burden, depending on how it’s written.Continue reading…

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Sites consistently strive to get, and stay on, the radar of sponsors and CROs for site selection. Improving this process is a goal of all sites regardless of their size and experience, but it can feel like a mysterious process to manage. Deirdre BeVard will bring her experience and insights from both the sponsor and site perspective to help bridge the gap in expectations and tips for how to overcome them.Continue reading…

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The challenges sites are faced with in meeting enrollment goals are undeniable. There are several factors that contribute to this challenge such as site location, lack of marketing, study awareness, and narrow eligibility criteria. Once you address and overcome these barriers, the next challenge is keeping your subjects interested. To do this, your site will need to have the proper structure in place to ensure you are positioned to meet your enrollment goals.Continue reading…

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As of May 2018, the EU General Data Protection Regulation applies to clinical trial data generated in the EU. What is the consequence of this EU regulation? How does it affect our trials?Continue reading…

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The force of Mother Nature is one that can’t be avoided or thwarted. This reality means that sites must have a well-designed and coherent Disaster Recovery Plan (DRP), otherwise known in the clinical research industry as a Disaster Plan SOP.Continue reading…

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