Clinical Investigator Training

As a clinical investigator involved in a clinical trial, you will be responsible for ensuring that the investigation is conducted according to the signed investigator statement, the investigational plan, and applicable regulations such as Good Clinical Practice (ICH GCP).    You will be responsible for protecting the rights, safety, and welfare of patients under your care; and for the control of drugs under investigation.

The training offered by Clinical Research Training will be of real value to you in your role as an investigator.  It gives you the chance to cover critical parts of your learning and development without detracting from your role of investigator, from your clinical role or from your management obligations.

Clinical Research Training offers you the chance to demonstrate your understanding and to gain a recognized certificate covering Good Clinical Practice.  The training takes place at a time and location that suits you fitting around your current obligations inside and outside of your working environment.  The courses are detailed, yet straightforward, enough to ensure you get all the information that you need to remain compliant with current legislation.  This is supported by methods that test your knowledge and understanding. 

E-learning means that your staff involved in the trial do not have to attend training courses at critical times.  Training can be tailored to the needs of the trial, upon your needs as the investigator and to the needs of the individual.

You can get the training that you need as the Clinical Investigator.  If you like it, Clinical Research Training courses can be used to ensure that the whole team involved in delivering the investigational plan attain the same standards in particular area of clinical research. 

At last, you can ensure that everyone involved in the trial has attained the same standard of knowledge and understanding.  Everyone has the same certification, particularly in ICH GCP, meaning that you can conduct the trail safe in the knowledge that you are fully compliant with MHRA regulations in this area.