Clinical research now takes place in every continent around the globe, offering the trialling of treatments for a huge range of diseases and conditions. These trials are a significant part of advancing medicine in countries all around the world, offering new hope and solutions for illnesses that claim thousands of lives each year.
There are several important elements to successful clinical research trials, and one of these is hiring a reliable and efficient Site Management Organisation (SMO). These organisations are often hired by sponsors or Clinical Research Organisations (CRO) in order to run clinical trial sites. The reason for this is that they offer several major benefits to research as a whole.
The importance of a quality SMO for clinical research starts with the increased level of efficiency that can be brought to proceedings, with the SMO providing management and support to the trained staff of the CRO. The staff at the SMO can be tasked with numerous roles, each helping experienced and trained investigators to focus on essential work.
There are many different aspects necessary for the successful carrying out of clinical trials, including data management, recruiting and enrolling people on clinical trials, administrative tasks and much more. The support that one of these organisations can provide to the CRO is significant and can allow clinicians to focus their attention on more important tasks.
The next area where SMO for clinical research can excel is by helping improve and maintain patient enrolment and retention rates for trials. This can be one of the most difficult parts of the whole clinical research process, with appropriate incentives needing to be in place in order to encourage participation.
Many experts have highlighted and praised the role of SMOs in the processes they have in place to recruit and encourage patients to stay on course throughout the entirely of clinical trials. Again, this is due to the organisation’s special role as a facilitator and aide to the Clinical Research Organisation that is directing the research.
More participation means that more valid results are able to be obtained, which can then lead to new, effective treatments being available for use much more rapidly. Even in countries where participation and enrolment is generally quite low, hiring an SMO has been consistently shown to make a significant improvement in retention rates.
Another area where SMO for clinical research has been particularly useful in developing nations or regions where clinical trials have not been carried out before on a large scale. For CROs looking to carry out research in these areas, SMOs can often provide legislative advice and guidance that can ensure that research is organised and conducted efficiently.
As clinicians in many of these developing regions many be unfamiliar with protocol and procedure, a Site Management Organisation can ensure that rules and regulations are being adhered to in order for results of research to be valid.
In some cases, SMOs can also offer training for those who are new to the field which can help establish new markets for clinical research in regions around the world. Indeed, some of the leading SMOs today have helped develop markets in Latin America and in Asia which have brought great benefits to clinical research as a whole.
The role of a quality SMO for clinical research has become critically important, from that the role that these organisations play in developing markets for research to helping trials run more efficiently. Many CROs and sponsors do well by finding reputable and reliable SMOs to work with in order to get the best results from their clinical research projects and endeavours around the world.