Mahesh Shinde Email & Phone Number | Over 10 years working in Clinical Research with the last 5 years in Clinical Project Management managing large global/multinational studies (Phase III) and 5 years as a Clinical Research Associate. Has significant experience working in Breast cancer, Renal cancer, Rheumatoid Arthritis, Paediatric and adult Asthma, Gastroesophageal reflux disease, Diabetes, Diabetic Nephropathy and Candidemia. Responsibilities included execution of the assigned medium to large multi country studies per Contract, from initiation through to closeout. Establishing clinical tools and processes for the study team for execution of clinical deliverable within study timelines identify quality issues within the study through regular review and ongoing training and support to the clinical team. Ensure that all project deliverables are completed to the Sponsor’s satisfaction, ensuring quality deliverables on time and within budget and in accordance with SOPs, policies and practices. Joined Global Process Delivery Center dept. (parallel movement) In Jan 2014, responsible for centralising the processes in India, closely working with all Global CPMs.

Mahesh Shinde

Over 10 years working in Clinical Research with the last 5 years in Clinical Project Management mana...
Mumbai, Maharashtra, India

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Mahesh Shinde’s Email mahesh.shinde@iqvia.com

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Mahesh Shinde’s Location Mumbai, Maharashtra, India

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Clinical Project Manager

Present

Clinical Project Manager

2011-01-01 00:00:00 - Present

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Mahesh Shinde is a Over 10 years working in Clinical Research with the last 5 years in Clinical Project Management managing large global/multinational studies (Phase III) and 5 years as a Clinical Research Associate. Has significant experience working in Breast cancer, Renal cancer, Rheumatoid Arthritis, Paediatric and adult Asthma, Gastroesophageal reflux disease, Diabetes, Diabetic Nephropathy and Candidemia. Responsibilities included execution of the assigned medium to large multi country studies per Contract, from initiation through to closeout. Establishing clinical tools and processes for the study team for execution of clinical deliverable within study timelines identify quality issues within the study through regular review and ongoing training and support to the clinical team. Ensure that all project deliverables are completed to the Sponsor’s satisfaction, ensuring quality deliverables on time and within budget and in accordance with SOPs, policies and practices. Joined Global Process Delivery Center dept. (parallel movement) In Jan 2014, responsible for centralising the processes in India, closely working with all Global CPMs.