Koushik Bhandari Email & Phone Number | 5.5+ years of versatile experience in Clinical Research field. highly professional approach towards the assigned jobs and maintaining co-ordination between team. Proficient in handling trial responsibility throughout the data-management life cycle. Have thorough knowledge of end to end activities of CDM and have worked in set up, conduct and close out phase. Skilled in handling multiple projects simultaneously and ability to work in critical environment, to prioritize task and achieve project time lines with effective time management. Have also performed on site audit and IMP release before site initiation and system audit to ensure ICH, GCP and other regulatories compliance. Able to work both independently and in a team applying high level of interpersonal skills Specialities: Clinical data management, Quality Assurance (late phase), Clinical Trial Management, Oncology, Immunology, CNS trials. Skilled in EDC platforms - Rave Classic, Medidata Rave, bizNET, Inform.

Koushik Bhandari

5.5+ years of versatile experience in Clinical Research field. highly professional approach towards...
Bengaluru, Bengaluru, India

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Koushik Bhandari’s Email koushik.bhandari@iqvia.com

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Koushik Bhandari’s Location Bengaluru, Bengaluru, India

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Senior Clinical Data Coordinator

Present

Data Analyst

2021-04-01 00:00:00 - 2022-05-01 00:00:00

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Koushik Bhandari is a 5.5+ years of versatile experience in Clinical Research field. highly professional approach towards the assigned jobs and maintaining co-ordination between team. Proficient in handling trial responsibility throughout the data-management life cycle. Have thorough knowledge of end to end activities of CDM and have worked in set up, conduct and close out phase. Skilled in handling multiple projects simultaneously and ability to work in critical environment, to prioritize task and achieve project time lines with effective time management. Have also performed on site audit and IMP release before site initiation and system audit to ensure ICH, GCP and other regulatories compliance. Able to work both independently and in a team applying high level of interpersonal skills Specialities: Clinical data management, Quality Assurance (late phase), Clinical Trial Management, Oncology, Immunology, CNS trials. Skilled in EDC platforms - Rave Classic, Medidata Rave, bizNET, Inform.