The sponsors include with in them device manufacturers, pharmaceutical companies, investigators, CROs or the Clinical Research Organizations, and any other person who are holding IND which is referred to Investigational New Drug Application or those who are NDA which refer to New Drug Application. Contact a sponsor and apply for a job if you are experienced, having clinical trial conduct knowledge and the training. Thesis is more than enough to become a Clinical Trial Manager.
Duties of Clinical Trial Manager
What is the work of the Clinical Trial Manager? The Clinical Trial Manager shortly defines as CTM having big responsibilities and the heavy duties which are stuffed over by the manager of project. The duty of the Clinical Trial Manager will be designated by the VP that is by the vice President. This will happen only when the head of the project is a Vice President (VP). These responsibilities were described in writing regulation. The main job of the Clinical Trial Manager is that they have to make sure that the investigators of clinical site have all the materials which they need to be conducting the clinical trails. This act can be possible if only the interacting takes place with the site through the Clinical Research Organizations or personally. The case report form is given by the Clinical Trial Manager. They also do adequate monitoring, product investigation and all other sponsor who is supporting the site of investigator's clinical. This is very good to be selected for future.