Senior Clinical Programmer (Rave)

Added
7 days ago
Type
Full time
Salary
Salary not provided

Related skills

sas clinical trials data migrations veeva cdms medidata rave

๐Ÿ“‹ Description

  • Lead and execute Medidata Rave programming activities, including study builds, custom functions
  • Develop, validate, and maintain software solutions using established development procedures to meet
  • Prepare and maintain technical documentation covering specifications, coding, validation, annotated
  • Provide application administration and technical support for clinical systems and tools, including
  • Monitor application performance, workflow alerts, system errors, and programming defects
  • Coordinate system integrations, application updates, software upgrades, and user acceptance testing

๐ŸŽฏ Requirements

  • Five to seven or more years of overall professional experience in clinical programming, with at
  • Demonstrated experience in Medidata Rave programming and multiple aspects of clinical study build
  • Experience with clinical programming migrations, Publish Check, PPC, TSDV, and study build
  • Mandatory SDBE Rave certification.
  • Strong understanding of clinical data management systems, clinical trial workflows, programming
  • Experience supporting application administration, system integrations, software updates, user

๐ŸŽ Benefits

  • Remote working arrangement within India.
  • Full-time employment opportunity.
  • Opportunities to work on clinical programming projects supporting drug development and clinical
  • Professional development and career progression opportunities.
  • Access to technical training, therapeutic-area learning, and knowledge-sharing initiatives.
  • Supportive management, peer recognition, and a total rewards program.
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