Conducting site specific start-up activities & documentation.Coordinating site level Regulatory IRB/IEC activities.Coordinating Site Quality Visits & Site Initiation Visits.Coordinating Phase II, III, IV clinical trials, including participantrecruitment informed consent and data collection.Maintained study database, ensuring data accuracy and timely reporting tosponsors (e.g. iMedidata Rave).Facilitated communication between the study team, sponsors andregulatory authorities.I am currently delegated in a thesis program 'An observational studycharacterizing tumor cytogenetics in adult population treated on apediatric based regimen' in Tata Medical Centre. My duties entailcollection and storage of data, follow up of patients, ensuring accurateadministration of chemotherapy as a part of thesis protocol as advisedby the physician, to note any adverse events due to the same and informto the principal and keep track of patients.Officially performed data operations in National Data CollectingSoftware for Research in Oncology (e.g. OncoCollect).Coordinating and keeping track of the patient’s bio banking sampleswith the bio banking team for patient’s bio banking samples processingand preservation for further treatment resources.Being a part of the Multidisciplinary team where the patient's case isdiscussed to plan the treatment plan. Created a patient specifictemplates which includes various diagnostic reports related to thedisease based on which the clinicians decide the further treatment plan.Coordinating T-cell Project 2.0 International Registry and P.I initiatedEACODE-AML Study (e.g. OpenClinica, REDCap) - Including participantrecruitment informed consent and data collection, maintained studydatabase, ensuring data accuracy and timely reported to study team.Working as a Clinical Data Manager with collaboration of CMC velloreClinical Data Management team at Tata Medical Center, Kolkata.