Site Management Organization Survey
Site Management Organizations come in different shapes, sizes, flavors and
colors. some are constituent parts of contract research organizations (CROs) while
others are part of private equity-backed roll-up operations. Still, others may represent
independent standalone operations. Some employ physicians/clinical investigators and
do traditional site work (e.g. conduct studies) while many others oversee and manage
the process. Learn more about the Clinical Research Courses
An organization that provides clinical trial-based services to a clinical research
organization, a biotechnology company, a pharmaceutical company, or even a
clinical site is known as a site management organization. The site is generally a
hospital or a healthcare institution having adequate staff and infrastructure to meet
the requirements of the clinical protocols.
The site management organization (SMO) is responsible for contracts, submission of
relevant documents to the ethics committees and review boards, patient counseling,
patient recruitment, site initiation and close-out operations, informed consent forms,
patient follow-ups, making sure of protocol compliance, advising and alerting on
various matters, archival of trial-related documents and their maintenance, regarding
and taking suitable actions on multiple violations with respect to protocols, etc.
Conclusion
SMOs specialize in running clinical research courses sites. Outsourcing a clinical
research trial to an SMO can help global pharmaceutical companies, especially in
setting up a business as an SMO, will minimize their workload effectively and
efficiently. Many numbers of hospitals, experienced and well-qualified doctors, large
patient pool emblematizing chronic as well as infectious diseases, high savings in
cost, and easy recruitment of patients are leading to become a lucrative hub for
conducting global clinical trials.