Role & responsibilities Performing as Sub-investigator in the assigned clinical studies Reviewing study documentsPreparation of Clinical Raw dataProtocol, SOP and various Regulatory complianceProtocol/ICF/CSR reviewStudy initiation and ExecutionPre study document preparationDosing of the subjectsMonitoring the study process Preparation of confinement report, clinical updates & clinical summary reportCompilation of study documents as per protocolReview study documents and handing over to QA for review.Close the QA / Sponsors observation / queriesArchival & Retrieval of study documentsSubject safety follow-upServing as QC in the assigned clinical studies Performing pharmacy activities.EC submission of protocols and related activitiesPreferred candidate profile Knowledge of ICH - GCP Knowledge in Regulatory guidelines like CDSCO, USFDA, EMEA, WHO etc.,Communication skills