Susmita Gupta Email & Phone Number

Director Data Management @ Enveda Biosciences

View Susmita's Email & Phone Number

5 free lookup(s). No credit card required.

If you need more lookups, subscriptions start at $34 USD/month.

Susmita Gupta Location

Hockessin, DE, US

Susmita Gupta Work

Director Data Management @ (October 2025 - Present)
President - Clinical Research Scientist (Consulting) @ (January 2021 - Present)
Clinical Scientist and DM SME @ (January 2023 - January 2026)
Clinical Scientist Consultant @ (July 2020 - December 2020)
Sr. Clinical Scientist -Oncology - Merck @ (March 2017 - July 2020)
Clinical Trial Operations Manager @ (March 2015 - March 2017)
RAVE Architect and Database builder - Specialist @ Consultant at Johnson and Johnson (November 2014 - February 2015)
Sr. Manager, Programt lead: Global Data Managment @ (January 2013 - November 2014)
Sr. CDM Project Manager @ Endo Pharmaceuticals (January 2010 - January 2013)
Program data Manager: consultant at Pfizer @ (November 2007 - November 2009)
Sr. Clinical research Specialist @ (August 2006 - November 2007)
Team Lead Data managment @ Glaxo Smith Kline (January 2006 - September 2006)
Principal clinical research scientist @ Glaxo Smith Kline (May 2005 - January 2006)
Team Leader, Clinical Data Sciences @ Glaxo SmithKline (GSK outsource group (May 2006 - August 2006)
Team Lead DM @ (January 2005 - January 2006)
Sr. Clinical Data manager @ (August 2002 - April 2005)
Sr. Clinical Data Manager @ PPD Development (January 2002 - January 2005)
Sr. Clinical Data Manager @ Arracel (October 2001 - August 2002)
Sr. Clinical Data Manager @ Araccel Corp (October 2001 - August 2002)
Senior Clinical Data Manager @ PAREXEL International Corporation (May 2000 - October 2001)
Primary (Lead) Clinical Data Manager @ PAREXEL International Corporation (May 1997 - May 2000)
Sr. Clinical Data Manager @ Parexel, International (May 1997 - October 2001)
Quality Assurance Auditor @ Clintrials Research Inc (September 1996 - May 1997)

Susmita Gupta Education

Medidata, a Dassault Systèmes company
Medidata Certified Industry Consultant (Clinical research drug development)
2024-2025
CCDM: Society For Clinical data Management
CCDM (Clinical data management certification)
2009-2009
Campbell University
Clinical Research
1999-2002
Coe College
BA (Biology and Material Science)
1989-1993
Coe College
BA (Biology)
1989-1992
Coe College
Biology/Biological Sciences (General)
1989-1992
Mathematics and
1985-1989
Institute of Project Management
PMP
2015
Wake Forest University

Susmita Gupta Skills

21 CFR Part 11
Agile Methodologies
Analytical Skills
Biopharmaceuticals
Biostatistics
Biotechnology
Business Data Management
Business Process Improvement
CDISC
CRF design
CRO
CRO Management
CTMS
Cardiology
Change Management
Clinical Data Management
Clinical Development
Clinical Monitoring
Clinical Research
Clinical Study Design
Clinical Trial Management System (CTMS)
Clinical Trials
Computer System Validation
Cross-functional Team Leadership
Customer Relationship Management (CRM)
Data Management
Data Protection Manager
Data acquisition and Integration
Data surveillance, for Risk based Monitoring and Fraud detection
Drug Development
Electronic Data Capture (EDC)
FDA
GCP
Good Clinical Practice (GCP)
GxP
IND
Infectious Diseases
Inform
Leadership
Medical Devices
Medical Writing
Medidata RAVE administrator
Medidata RAVE architect Study builder
Medidata Rave
Oncology
Pharmaceutical Industry
Pharmacovigilance
Project Management
Quality Assurance
Regulatory Affairs
Regulatory Submissions
Therapeutic Areas
Trial operations project Management
U.S. Food and Drug Administration (FDA)
U.S. Title 21 CFR Part 11 Regulation
Vendor management
For Risk Based Monitoring and Fraud Detection
Ich Gcp
Clinical Trial Management System Ctms
Data Surveillance
Good Clinical Practice Gcp
Life Sciences
Oracle Clinical
Validation
Operations
Lifesciences
Protocol
Cross Functional Team Leadership
Pharmaceutics
u.s. Food and Drug Administration Fda
EDC
Management
Electronic Data Capture Edc
Sop
Good Clinical Practice
Electronic Data Capture
Clinical Trial Management System
u.s. Food and Drug Administration

Susmita Gupta Summary

Susmita Gupta, based in Hockessin, DE, US, is currently a Director Data Management at Enveda. Susmita Gupta brings experience from previous roles at CRST - CLINICAL RESEARCH SWAT TEAM LLC, Delcath Systems, Calithera Biosciences and ExecuPharm. Susmita Gupta holds a 2024 - 2025 Medidata Certified Industry Consultant in Clinical research drug development @ Medidata, a Dassault Systèmes company. With a robust skill set that includes 21 CFR Part 11, Agile Methodologies, Analytical Skills, Biopharmaceuticals, Biostatistics and more. Susmita Gupta has 2 emails and 1 mobile phone numbers on RocketReach.