To secure a responsible career opportunity to fully utilize my training and skills, while making a significant contribution to the success of the company.
Overview
7
7
years of professional experience
7
7
years of post-secondary education
1
1
Language
Work History
Clinical Programmer II
Syneos Health
Gurgaon
10.2021 - Current
Utilizes primary development tools including Veeva Vault CDMS for design data base.
Generates and maintains all required documentation, including the development of specifications, coding and validation efforts in support of annotated Case Report Forms (CRFs),
database creation, coding configuration, edit check procedures.
Create DVS document and share with Validation team.
Resource Management & Work Allocation.
Provide support to Data Management team for on ongoing studies.
Ensures quality deliverables by providing review of study level core deliveries for accuracy.
Used critical thinking to break down problems, evaluate solutions and make decisions.
Senior Process Associate
Tata Consultancy Service Ltd
Thane
04.2016 - 10.2021
Over Client/Server based application
Knows how to design electronic Case Report Forms to minimize data entry errors
Knows how to use the system to keep data clean and manage the data
Ability to articulate how the EDC process and the paper data collection process differ and overlap
Summary: 5 years of experience in Clinical Data Management.
CDMS: - Informs (v6.0,V6.2,V6.3), Central Designer (2.0,6.2,6.3)
Responsible for developing and maintaining clinical trial databases in EDC tool Inform
Study setup, Database Designing, Validation Procedures
Programming Inform checks
To analyze the issues faced in the clinical trial and to provide resolution
Creating Integrated Data Review Plan
Resource Management & Work Allocation
Provide support to Data Management team on ongoing studies
Creating the DVS according to the therapeutic area by using the template
IBM COGNOS TOOL (IE 8 and Above)
Deployed the Global core reports using the standard template
Develop study specific report as per study team requirements
Senior Lead Project Specialist – Global Clinical Trials & RWLP at Syneos HealthSenior Lead Project Specialist – Global Clinical Trials & RWLP at Syneos Health