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Clinical Database Programmer

Job Description

Must-Have**

(Ideally should not be more than 3-5)

Technical:

  • Review /update Study build specification documents.
  • Build/amend & Validate Study database as per the study build specification documents.
  • Program/modify checks/procedures as per the study build specification documents.
  • Update and upload the relevant documents on shared client portal on completion of the tasks.
  • Creates and maintains the Global Library
  • Update the database for any QC/User acceptance test findings.
  • Possess a strong knowledge on Object Oriented Programming concepts and C# Programming.
  • Hands on experience in MS Visual Studio and SQL Server
  • Knowledge for debugging Custom Functions
  • Reviews the Data Validation Specification documents and Categorizes the Edit Checks and Custom Functions
  • Has knowledge on various Simple to Complex Custom Functions.
  • Work with Standards team and suggest updates/deviations on Standard C ustom Functions used across studies.
  • Analyze the Custom Function related issues in Production and provide effective solutions on fixing those issues.
  • Performs the Peer Review of the Custom Function code developed by the other Custom Function Programmer
  • Understand the process of extracting CRF and non CRF data
  • Understand and identify the Reporter modules needed for a study
  • Create and execute programs based on Visits, eCRF and protocol to generate reporter modules
  • Behavioral:

  • Excellent writing, communication and customer handling skill
  • Confidence and ability to interface professionally with wide spectrum of customers
  • Works closely with SME/Development team and provide solutions/suggestions for the new requirements.
  • Solid multi tasking and problem resolution abilities
  • Self-motivation and self-drive: the individual must have the drive to do things on his/her own without being supervised
  • Good-to-Have

  • Build experience on multiple leading Clinical database
  • Understand the usage of CDISC SDTM guidance rules to annotate eCRFs with SDTM domains and variables
  • Posted
    06/23/2022
    Location
    bangalore, KA, IN