Chetankumar Kabbur
About Chetankumar Kabbur
Chetankumar Kabbur is a Global Trial Specialist at Bristol Myers Squibb in Hyderabad, India, with extensive experience in clinical research and trial management.
Professional Experience at Bristol Myers Squibb
Chetankumar Kabbur currently serves as a Global Trial Specialist at Bristol Myers Squibb in Hyderabad, Telangana, India. He began this role on November 1, 2023. His responsibilities encompass managing end-to-end clinical trial studies. These include site feasibility, budget management, IEC submission, site initiation, study conduct, clinical data management, EDC, IP, lab shipment, ISF management, eTMF, notification of AE & SAE, CTRI, and site close-out and archival activities.
Previous Roles in Clinical Research
Before his current role, Chetankumar Kabbur worked in various positions in clinical research and operations. From 2021 to 2023, he was a Clinical Trial Associate at Aurigene Oncology Limited in Bengaluru. Prior to that, he served as an Associate in Clinical Operations at IQVIA for one year. He also has experience as a Clinical Research Coordinator at both ST. JOHN'S MEDICAL AND RESEARCH CENTER (2019-2020) and KLES DR Prabhakar Kore Hospital & MRC (2018-2019). His early career includes a role as an Executive Assistant at GENO PHARMACEUTICALS PVT LTD (2016-2017) and Unilabs (2014-2016).
Education and Academic Background
Chetankumar Kabbur holds a postgraduate degree in Clinical Research, which he achieved from Kle College of Pharmacy, Belgaum, from 2017 to 2019. He also possesses a Bachelor of Nursing degree, obtained from the College of Nursing, KIMS Hubli, between 2010 and 2014. Throughout his academic career, he developed a deep expertise in managing clinical trials and healthcare research.
Clinical Trial Expertise
Chetankumar Kabbur has specialized expertise in managing various aspects of clinical trial studies. His skills include handling end-to-end clinical trial activities such as site feasibility, budget management, IEC submission, site initiation, study conduct, clinical data management, electronic data capture (EDC), investigational product (IP) management, lab shipment, ISF management, eTMF, notification of adverse events (AE) and serious adverse events (SAE), CTRI registration, and site close-out and archival activities. He is experienced in conducting Phase I, II, III, IV, and PK/PD global trials, bringing a comprehensive understanding of clinical research processes.
Background in Nursing
Chetankumar Kabbur's foundation in the healthcare field is supported by his undergraduate degree in Nursing Science from the College of Nursing, KIMS Hubli, awarded by RGUHS University. This academic background has provided him with essential healthcare knowledge that complements his capabilities in clinical research and trial management. His nursing experience adds a valuable perspective to his current role and responsibilities.