To prepare the Annotation CRF using Skilled Adobe Acrobat.
SDTM and ADaM Programming as per CDISC Guidelines
Creation of SDTM and ADaM mapping specification sheet, modify and maintain SAS programs.
To prepare CDISC database as per CDISC standards and regulatory deliverables. (Define xml., SDTM aCRF).
Creation/Modification of Macros for repetitive tasks
To use SAS Macro for repetitive tasks.
Metadata and Define.xml file creation
To Create Metadata and define.xml file (Using Pinnacle 21)
cSDRG and ADRG Guide Preparation
To prepare the cSDRG and ADRG report as per FDA guideline.
Validation of CDISC (SDTM and ADaM) outputs
Identify and edit checks as per the data validation
To Run Pinnacle 21 validator on clinical trial data and troubleshoot finding with stakeholder.
SOP Training
To complete internal SOP/CLP training as in timely manner
QA response with in the timelines
To provide QA response within the timelines.
📌 Sas Programmer Gujarat (India)
🏢 Veeda CR
📍 India
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.