The position

As a CTA, you will provide support to the CDC Trial Managers and CRAs in relevant aspects of trial activities in CDC-India (start-up, execution and closure) and facilitate timely clinical project deliverables of required quality by Novo Nordisk India in accordance with Good Clinical Practice (GCP) guidelines and in line with local regulatory requirements.The scope of CTA activities for a particular clinical trial may vary with respect to countries sponsored. The activities start post country allocation and ends after study documents are sent for central archival post completion of trial. In this role your main responsibilities will be customization and translations of study documents, Health Authority and Ethics Committee submissions, contracts, auxiliary and trial product supplies management, support for arranging global/local investigator meeting and other departmental meeting or related activities, study payments, systems, filing of study document...