Clinical Trial Management Statistics


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Clinical Trial Management Statistics 2023: Facts about Clinical Trial Management outlines the context of what’s happening in the tech world.

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Top Clinical Trial Management Statistics 2023

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Clinical Trial Management “Latest” Statistics

  • Approximately 40% of clinical trials are supported by noncommercial sponsors, mostly academics, and the pharmaceutical sector funds 60%.[1]
  • 97% of those that responded and used new techniques for clinical trials during the pandemic said their organization would continue to use at least one of these new techniques.[2]
  • 58% of respondents, a small majority, said that their organizations intend to provide patients with the choice of how they participate in clinical studies.[2]
  • The COVID-19 pandemic, according to 76% of respondents in an industry poll conducted by Informa Pharma Intelligence and Oracle last year, has increased the use of decentralized clinical trial approaches.[2]
  • Most survey participants anticipate a rise in fit-for-purpose, hybrid, and/or decentralized clinical trial models in the future, 63% of whom expect these models to be utilized for both new studies and the restarts of current trials.[2]
  • Survey participants who used novel clinical trial techniques during the pandemic anticipated their organizations would utilize hybrid models more often (44%) and fit-for-purpose models more frequently (42%).[2]

Clinical Trial Management “Other” Statistics

  • The compliance rate increased between April 2019 and June 2022 from 24% to 64% for noncommercial sponsors to 77% to 86% for commercial sponsors.[1]
  • Among the four models: evaluated, site-based, fit-for-purpose, hybrid, and decentralized models, respondents expect a 24% drop in site usage.[2]
  • A whopping 87% of survey participants reported being able to utilize most or all of the extra data their recently deployed procedures have produced.[2]
  • 76% of responses were from biopharmaceutical businesses, while the remaining respondents were from medical device companies and CROs.[2]

Also Read

How Useful is Clinical Trial Management

One of the key benefits of clinical trial management is ensuring that trials are conducted ethically and in compliance with regulatory requirements. Research involving human subjects must adhere to strict ethical standards to protect the rights and safety of participants. Clinical trial managers play a crucial role in ensuring that these standards are met and that trials are conducted in an ethical manner. Additionally, they are responsible for ensuring that trials comply with regulations set forth by regulatory bodies such as the Food and Drug Administration (FDA) in the United States and the European Medicines Agency (EMA) in Europe.

Another important aspect of clinical trial management is effective communication and collaboration among all stakeholders involved in the trial. This includes researchers, physicians, study coordinators, data managers, regulatory authorities, and sponsors. Having clear lines of communication and a well-coordinated team is essential for the successful implementation of a clinical trial. Clinical trial managers are often the glue that holds these diverse stakeholders together, ensuring that everyone is working towards a common goal and that any issues or challenges are addressed in a timely and efficient manner.

Furthermore, effective data management is a critical component of clinical trial management. Clinical trials generate large amounts of data that must be collected, stored, analyzed, and reported in a consistent and accurate manner. Clinical trial managers are responsible for overseeing the data management process, ensuring that data is collected in accordance with the study protocol, and that it is of high quality. This is essential for ensuring the validity and reliability of the trial results and for ultimately determining the safety and efficacy of the intervention being studied.

In addition to managing the operational aspects of clinical trials, clinical trial managers also play a key role in ensuring that trials are completed on time and within budget. Clinical trials are complex endeavors that require careful planning and execution, and any delays or overruns in the timeline or budget can have serious implications for the trial and its outcomes. Clinical trial managers are responsible for monitoring progress, identifying potential risks and challenges, and developing strategies to mitigate these risks and keep the trial on track.

Overall, clinical trial management is a critical component of the drug development process and is essential for ensuring the safety, quality, and integrity of clinical trials. Without effective and efficient clinical trial management, the process of bringing new treatments and medications to market would be chaotic and unreliable. Clinical trial managers play a vital role in coordinating the many moving parts of a clinical trial and ensuring that the trial is conducted in a rigorous and ethical manner. Their expertise and dedication are essential for advancing medical science and improving the health and well-being of patients around the world.

Reference

  1. europa – https://www.ema.europa.eu/en/human-regulatory/research-development/clinical-trials-human-medicines
  2. oracle – https://www.oracle.com/industries/life-sciences/clinical-research/clinical-trials-post-covid-research/

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