![]() So, to maximize your recruitment budget, it’s important to find ways to speak directly to patients. Studies show that although doctors and nurses feel comfortable discussing clinical trials with their patients, they only refer 0.2% of patients to relevant studies. Get socialĬompetition for patients to take part in trials is making researchers think outside the box – and innovating beyond traditional recruitment methods may also be cheaper and more efficient. By keeping patients on board as your trial progresses, you won’t need to continually recruit. PrioritiZe patient engagementĮngaging with patients taking part in your trial isn’t considered a priority for many but investing in effective communication with participants could help to improve retention. With the CDM market growing at a healthy 13% and forecast to reach 14.7% in 2025 it seems more researchers are choosing to go digital. Increasing the use of technology like CDMs can help you to plan and budget more effectively. Technologies like Clinical Data Management systems are helping researchers to manage multiple data points, improving the way they conduct trials. Invest in a clinical trial data management (CDM) system Working with an experienced and knowledgeable partner is key - so choose wisely. Timely delivery of supplies across all sites can help you avoid any unnecessary delays. However, in the clinical trials supplies market it's quality, not cost, that should be the determining factor. The growth is positive, with new entrants increasing competition. The global clinical trials supply market is growing at almost 7% a year. As such, senior research fellow at the Tufts Center for the Study of Drug Development, Mary Jo Lamberti, Ph.D., believes that sharing information on the most effective sites within your organization (and potentially with others) can help you to identify the most effective sites. Recent research has found that up to 11% of all multi-center trial sites aren’t activated. It can cost between $20 - $30,000 to initiate each site, with maintenance costs of up to $1,500 per month. Having a solid CTA in place before you approach sites can help you to manage this process efficiently, saving precious budget. The increase in the number of trials means there is greater competition for site locations, which can make identification and negotiation a time-consuming process. Have effective Clinical Trials Agreements (CTAs) in place ![]() Do your research and choose only those with a proven history of delivery. The market for CRO services is buoyant, but it’s worth picking a partner wisely. Outsourcing is a trend that shows no signs of slowing, as companies seek to cut costs by conducting trials in more cost-effective locations. The right CRA can keep site staff grounded and engaged, ultimately serving to meet the goals of both the CRO and the sponsor.” Being willing to invest in the right CRA can ultimately help you maximise your budget further down the line. According to Maria Ladd, Senior Manager, Global Study Start-Up, inVentiv Health, “The CRA/site relationship is a critical factor in the overall clinical trial process. In practical terms, you may need to increase wages, but this will likely be offset by avoiding delays. Think long term and invest time and resources in attracting the right staff and work hard to keep them. ![]() One recent investigation found 14,000 CRA roles advertised across the world. The worldwide shortage of Clinical Research Associates is increasing demand and pushing up wages. Make sure to include known variables like inflation. In March 2020, there was around a 65% global average decrease in the enrolment of new patients year-over-year, so include a contingency large enough to accommodate any potential problems like protocol amendments, recruitment issues or difficulties managing outsourced vendors. It’s impossible to plan for unforeseen occurrences that can stall your trial – but you can budget for them. Scientists, it seems, tend to underestimate the cost of clinical trials – in some cases by up to 16%. Here are 10 ways that you can maximize your budget and minimize delays. The reality is that 85% of clinical trials will experience delays and the impact on budgets can be huge. Set-up times are being increased by trends such as the growth of multi-site and multi-country trials in a sample of 400 trials, researchers found that the average time taken for commencement was between 5-6 months. The average cost of developing a new drug has reached a staggering $2-3 billion so it’s no wonder that clinical trial researchers are looking for ways to tighten up and make their budgets stretch further. Running a clinical trial in 2021 is tougher than ever.
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