ISCR has ten functioning councils which constitute the major activities of the Society. Each of the Councils has a Council Coordinator and Members who drive the respective agenda of the Councils, guided by the overall objectives and mission of the Society.

An Investigator is responsible for the conduct of the clinical trial at a trial site. The trial site is the location(s) where most of trial-related activities are actually conducted. Therefore, the investigator and his/her team are an important stakeholder in a clinical trial. An investigator is expected to comply with all the responsibilities as laid out in the ICH GCP guidelines and the applicable regulations.

Key opinion leaders / highly experienced clinical trial investigators represent the investigator community, on the Investigator Council of ISCR.

• Investigator SOP
• Information Repository
• Investigator Helpline
• Insight Newsletter