Bhaskar Jyoti... Email and Phone Number

25.06.08 Responsibilities-Assist in the compilation of the study related documents during the pre trial PeriodAssisting study managers for start up activities & site initiationRecruitment & Retention of patientsAssist in the process of administering the informed consent to potential patients and discussing in detail the patient information sheetFollow up with site team for timely completion of the Source Documents and ensuring that all the relevant information… Show more 25.06.08 Responsibilities-Assist in the compilation of the study related documents during the pre trial PeriodAssisting study managers for start up activities & site initiationRecruitment & Retention of patientsAssist in the process of administering the informed consent to potential patients and discussing in detail the patient information sheetFollow up with site team for timely completion of the Source Documents and ensuring that all the relevant information required in the Case Record Form are present in the source documentComplete the Case Record Forms within the timelines and with minimal errorsSchedule subject visits as per the protocol to ensure maximal subject compliance retentionCoordinate all lab related activities - shipment of samples through the designated courier and ensure timely receipt of the lab reportsCoordinate with IP shipment processCompile and update the Trial Master FileMaintain the study related logs - screening, enrolment, drug administration, temperature and other communication logsManage the accountability of the Clinical Trial MaterialCoordinating Ethics Committee Submission & ApprovalCoordinate for any query from the Ethics CommitteeData query resolution raised by Data Management Show less