Sandeep Mohanty
Myself Clinical Research Professional with 6.2years of Core Regulatory Affairs Exp. & CTA Experience from IQVIA, GSK &... | Bengaluru, Karnataka, India
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Sandeep Mohanty’s Emails sa****@ca****.ai
Sandeep Mohanty’s Phone Numbers No phone number available.
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Sandeep Mohanty’s Location Bengaluru, Karnataka, India
Sandeep Mohanty’s Expertise Myself Clinical Research Professional with 6.2years of Core Regulatory Affairs Exp. & CTA Experience from IQVIA, GSK & TCS-Az-Maestro respectively. Currently working as Senior Regulatory Submission Publisher and Lead Reviewer with Coordinator role for all markets mostly EU market with submission via eCTD and NeeS format at Parexel.
Sandeep Mohanty’s Current Industry Liquent A Parexel
Sandeep
Mohanty’s Prior Industry
Liquent A Parexel
|
Quintiles
|
Iqvia
|
Glaxosmithkline Pharma
|
Tata Consultancy Services
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Work Experience
Liquent A Parexel
Senior Regulatory Affairs Associate
Wed Sep 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Tata Consultancy Services
Senior Process Associate
Tue Oct 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Sep 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Glaxosmithkline Pharma
Nce Cta Submission Coordinator
Sat Dec 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Sep 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Iqvia
Senior Site Management Coordinator
Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Dec 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Iqvia
Clinical Process Associate-1
Sat Oct 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Dec 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
Quintiles
Clinical Process Trainee
Tue Mar 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Sep 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Liquent A Parexel
Senior Regulatory Affairs Associate
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Sandeep Mohanty Email Addresses
FAQ About Sandeep Mohanty
-
Sandeep Mohanty is located at
Bengaluru, Karnataka, India -
Sandeep Mohanty is a
Myself Clinical Research Professional with 6.2years of Core Regulatory Affairs Exp. & CTA Experience from IQVIA, GSK & TCS-Az-Maestro respectively. Currently working as Senior Regulatory Submission Publisher and Lead Reviewer with Coordinator role for all markets mostly EU market with submission via eCTD and NeeS format at Parexel. Liquent A Parexel -
Sandeep Mohanty currently works in the
Liquent A Parexel -
Sandeep Mohanty specializes in
Myself Clinical Research Professional with 6.2years of Core Regulatory Affairs Exp. & CTA Experience from IQVIA, GSK & TCS-Az-Maestro respectively. Currently working as Senior Regulatory Submission Publisher and Lead Reviewer with Coordinator role for all markets mostly EU market with submission via eCTD and NeeS format at Parexel. -
Sandeep Mohanty speaks the following languages:
No languages available. -
Sandeep Mohanty has prior experience in the following industries:
Tata Consultancy Services , Glaxosmithkline Pharma , Iqvia , Iqvia , Quintiles -
Sandeep Mohanty has the following professional experience:
Liquent A Parexel , Tata Consultancy Services , Glaxosmithkline Pharma , Iqvia , Iqvia , Quintiles , Liquent A Parexel . -
You can view Sandeep Mohanty’s
LinkedIn profile at LinkedIn URL. -
Sandeep Mohanty’s work email addresses are
[email protected] . -
Sandeep Mohanty works at
Liquent A Parexel
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