The role of a study nurse can be adjunctive to other responsibilities within the hospital or the practice or can be the sole and dedicated professional activity. Then, it can be limited to the duration of a study and the profession can be carried out on a free-lance basis, or it can be full time and center linked.
For the development of new molecular entities, several well-controlled clinical studies are necessary during the overall lengthy clinical research process. These studies are done by Physicians, called Investigators when participating in a clinical studies, be it in a hospital setting or in a private practice. While it is the responsibility of the Investigators to carry out the final patient selection and their treatment, many tasks within a clinical study are delegated to a study nurse who takes a significant role in handling the direct patient communication, administrative matters, drug accountability and often the main communication to the sponsor pharma company, the contract research organisation or the site management organisation. A good study nurse is often the organisational manager of a study.
Clinville is a dedicated Investigational Site Management Organisation with a network of independent practising physicians conducting clinical studies by using web-based data management (e-trials). E-trials allow to perform studies fester and to a higher level of quality with less time consuming monitoring and data clarification workload.
Study Nurse Training
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