Sandhya Pulla

Angestellt, Clinical Data Standards Analyst, GlaxoSmithKline

London, Vereinigtes Königreich

Fähigkeiten und Kenntnisse

With more than 10 years of experience in Pharma do

Good experience in creating SDTM datasets and mapp

Good understanding of CDISC SDTM Implementation Gu

Trials proficient in designing and developing eCRF

Writing and implementing data validation checks by

Thorough knowledge of Clinical Trials data.

Good knowledge in different phases (phase I to III

Bis heute 7 Jahre und 6 Monate, seit Jan. 2017
Clinical Data Standards Analyst
GlaxoSmithKline
I was part of the team to convert internal GSK standards to CDISC SDTM standards. I provided support for the development and maintenance of GSK SDTM mappings, including Controlled Terminology (CT) mappings. These mappings provide instruction for transforming GSK legacy (IDSL) standards to CDISC SDTM standards.
5 Jahre, Aug. 2010 - Juli 2015
Clinical Database programmer
Cmed Research
As a clinical database programmer should liaise with the customers to configure trial databases and providing expert support and advice in implementing Timaeus within their environment. Configuration of Timaeus databases (screen design, visit definition and programming edit checks, derivations and functions) according to client’s specifications and within agreed delivery timeframes.
1 Jahr und 2 Monate, Juni 2009 - Juli 2010
Study Services Analyst
PAREXEL International GmbH
Design and development of eCRFs using DataLabs as per study protocol specification, accommodate any specter changes.
1 Jahr und 2 Monate, Jan. 2008 - Feb. 2009
InForm Programmer
GlaxoSmithKline

4 Jahre und 6 Monate, Jan. 2001 - Juni 2005
Electrical engineering
JNTU Hyderabad

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