Programmer - RAVE

IQVIA India

Bengaluru

Hybrid

INR 800,000 - 1,400,000

Full time

14 days+

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Job summary

IQVIA India seeks a software professional with Medidata Rave experience to design and implement edit checks and custom functions in C#. The role requires understanding of EDC and basic GCP concepts, with a goal to improve data validation and client satisfaction.

Candidates should have at least 2 years of applications programming experience, and be capable of building internal tools for quality metrics using Excel and Visual Studio while working in a hybrid environment across India.

Qualifications

  • Read and program Medidata Rave edit checks and custom functions from data specs.
  • Strong understanding of EDC systems and GCP basics.
  • Minimum 2 years of applications programming experience.

Responsibilities

  • Perform postproduction changes and validations to ensure data integrity.
  • Provide suggestions and solutions to operational issues as they arise.
  • Interact with corporate and CDM teams to negotiate timelines, responsibilities and deliverables.
  • Build internal tools for quality metrics using Excel, Visual Studio or similar platforms.
  • Work independently and complete projects with minimal supervision.

Skills

Rave
Custom Function
C# Programming
EDC

Tools

Visual Studio
Excel

Job description

Work location: Any IQVIA office Location in India

Work Mode: Hybrid

Must Have Skills: Rave and Custom Function is a must

Job Description
  • Read, Understand and program Medidata Rave Edit checks and custom function (C# Programming) from Data validation specification which meets Client requirement
  • Good working understanding of EDC. Qualification
  • Incumbent possesses and has demonstrated basic knowledge of systems and programming with minimum of two (2) years of applications programming experienc
  • As an alternative to the experience requirements listed above, possesses sufficient specialization
  • Information Technology experience to result in a specific Technology Experience Ratio of 25-50% (years of experience in the specific technology years the technology has existed)
  • Good Clinical knowledge including GCP and other standard practices
  • Perform postproduction changes
  • Provide suggestions and solutions to operational issues
  • May interact with corporate team and CDM team members to negotiate timelines, responsibilities, and deliverables
  • Build internal tools for quality and other similar metrics using various tools (Excel, Visual studio or any other platforms)
  • Ability to work independently and complete projects with minimal supervision
  • Sound understanding of coding and development processes
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