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Clinical research (CR) directors who hope to improve staff retention and motivation might begin by keeping the lines of communication open with principal investigators, clinical trial coordinators, and the rest of the research team.
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In clinical research documentation, the little things definitely count and often could lead to major regulatory problems.
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Clinical trial data increasingly is collected and communicated electronically. Sites often are dependent on how sponsors and clinical research monitoring organizations set up their data collection and editing systems, but there are issues they can prevent through better processes and preparation.
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Often overshadowed by other pressing clinical research needs, the detailed, difficult process of data management is drawing closer scrutiny by the Food and Drug Administration, researchers are finding.
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Research institutions continually look for ways to make their operations more efficient, especially during lean economic times.
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The Office for Human Research Protection (OHRP) has made educational videos available for the first time on the U.S. Department of Health and Human Services' YouTube channel.
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One of the chief benefits of installing an electronic IRB system is that it will automatize many of the standard administrative duties for IRBs and give managers and staff more time for work that will enhance human subjects protection.
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A project in Nashville, TN, to engage the community in cancer clinical trials has borne more fruit than its organizers had initially hoped.