• Perform investigator site visits, manage investigator sites between visits• Collect Site Regulatory Documents and perform primary Quality Control of SRD• Assure adherence to the protocol, GCP, SOPs and take necessary action to bring about compliance• Handle CRFs and DCFs and perform in-house CRF review• Facilitate adverse event reporting• Assist in preparation for and to participate in Investigator meetings and participate in study team meetings• Maintain a site specific part of the Trial Master File• Perform responsibilities of the Medical Supervisor in Study Team• Supervise and train CRAs Entry Level