Siara understands the need for highly trained and skilled clinical Investigators partnering pharmaceutical and biotechnology companies. Training ensures that investigators and their site staff understand and can apply provisions to protect the rights, safety, and well-being of study participants.
With this in mind Siara has developed Investigator training to nurture Investigators and sites into ‘centres of excellence’ for clinical research. Below is a selection of workshops available for Investigators and Site Staff.
Below are a few examples of the Sponsor Solutions offered by Siara.
This 2 Day workshop would set the foundations on understanding the requirements of ICH GCP and on how to successfully conduct a clinical trial, ensuring the safety, rights, well being of the trial subjects are protected and the data that is produced from the clinical trial is complete accurate and unbiased.
It is recommended that this 2-Day workshop be attended by all key site staff (Investigators, Sub-Investigators and Study Coordinators).
This 1 day workshop provides the practical skills needed to construct and negotiate study budgets that appropriately compensate investigative sites for resource needs required as a result of clinical research protocols.
Protection of human rights is one of the fundamental principals of GCP. This 1 Day workshop will discuss the history of informed consent, the development of the informed consent form and the informed consent process.
The Inspector is coming! The key to effective management of regulatory inspections is preparation. This 1 day workshop will give an insight into what regulatory inspectors look for during an inspection and how the investigator should prepare for a regulatory inspection.