Shilpa Kusum Dhadiga
Service and results-oriented researcher with over 12 years of experience in global Pharma Industry and a Master’s degree... | Greater Sacramento, Greater Sacramento, United States
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Shilpa Kusum Dhadiga’s Emails sh****@sf****.com
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Shilpa Kusum Dhadiga’s Location Greater Sacramento, Greater Sacramento, United States
Shilpa Kusum Dhadiga’s Expertise Service and results-oriented researcher with over 12 years of experience in global Pharma Industry and a Master’s degree in Biotechnology from University of Greenwich, London. Experienced with determining the product and portfolio level standards for clinical development planning, scientific document content, data analysis and reporting. Ensure program specific standards are developed and implemented across all trials to achieve consistency of the clinical dossier. Thorough knowledge of GCP, regulatory and decentralized clinical trial process. Exceptional Project Management skills and operational experience in planning, executing, and reporting clinical trials within study budgets. Directly supervised clinical research associates and conducted training.
Shilpa Kusum Dhadiga’s Current Industry Icon
Shilpa
Kusum Dhadiga’s Prior Industry
University Of Greenwich
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Nhs England
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Lab Services Watford Pharmaceticals
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Hetero Biopharma
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Hetero Usa
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Sf Research Institute
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Cvs Health
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Eli Lilly
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Work Experience
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Clinical Trial Project Manager/Clinical Operations Study Lead
Tue Nov 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Eli Lilly
Clinical Trial Project Manager
Tue Dec 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Feb 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
Cvs Health
Clinical Study Manager
Wed Jul 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Dec 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)
Sf Research Institute
Clinical Trial Project Manager and Business Development Lead
Mon Jul 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jul 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)
Hetero Usa
Clinical Trials Management Associate
Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jun 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Hetero Biopharma
Medical officer in Clinical Development & Medical Affairs
Fri Apr 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Dec 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
Lab Services Watford Pharmaceticals
Quality Control Manager
Fri May 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Mar 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Lab Services Watford Pharmaceticals
Lead Clinical Research Coordinator
Fri Mar 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Apr 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)
Nhs England
Clinical Research Associate
Wed Feb 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Feb 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Nhs England
Clinical Research Coordinator
Sun May 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
University Of Greenwich
Research Assistant and Analytical Scientist
Wed Sep 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Apr 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Shilpa Kusum Dhadiga Email Addresses
FAQ About Shilpa Kusum Dhadiga
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Shilpa Kusum Dhadiga is located at
Greater Sacramento, Greater Sacramento, United States -
Shilpa Kusum Dhadiga is a
Service and results-oriented researcher with over 12 years of experience in global Pharma Industry and a Master’s degree in Biotechnology from University of Greenwich, London. Experienced with determining the product and portfolio level standards for clinical development planning, scientific document content, data analysis and reporting. Ensure program specific standards are developed and implemented across all trials to achieve consistency of the clinical dossier. Thorough knowledge of GCP, regulatory and decentralized clinical trial process. Exceptional Project Management skills and operational experience in planning, executing, and reporting clinical trials within study budgets. Directly supervised clinical research associates and conducted training. Icon -
Shilpa Kusum Dhadiga currently works in the
Icon -
Shilpa Kusum Dhadiga specializes in
Service and results-oriented researcher with over 12 years of experience in global Pharma Industry and a Master’s degree in Biotechnology from University of Greenwich, London. Experienced with determining the product and portfolio level standards for clinical development planning, scientific document content, data analysis and reporting. Ensure program specific standards are developed and implemented across all trials to achieve consistency of the clinical dossier. Thorough knowledge of GCP, regulatory and decentralized clinical trial process. Exceptional Project Management skills and operational experience in planning, executing, and reporting clinical trials within study budgets. Directly supervised clinical research associates and conducted training. -
Shilpa Kusum Dhadiga speaks the following languages:
No languages available. -
Shilpa Kusum Dhadiga has prior experience in the following industries:
Eli Lilly , Cvs Health , Sf Research Institute , Hetero Usa , Hetero Biopharma , Lab Services Watford Pharmaceticals , Lab Services Watford Pharmaceticals , Nhs England , Nhs England , University Of Greenwich -
Shilpa Kusum Dhadiga has the following professional experience:
Icon , Eli Lilly , Cvs Health , Sf Research Institute , Hetero Usa , Hetero Biopharma , Lab Services Watford Pharmaceticals , Lab Services Watford Pharmaceticals , Nhs England , Nhs England , University Of Greenwich . -
You can view Shilpa Kusum Dhadiga’s
LinkedIn profile at LinkedIn URL. -
Shilpa Kusum Dhadiga’s work email addresses are
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Shilpa Kusum Dhadiga works at
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