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Clinical Programmer

Clinical Ink
Remote, USA
Full-time
Senior Level
Remote
Discovered 1 months ago

Full Job Posting

  • Review and apply data mappings for customer specific data exports
  • Perform peer review / QC of data export programming
  • Produce data transfers via data export files and/or web services
  • Work with customers to specify data transfer standards and develop/implement software code to automate data transfer activities
  • Provide database programming support for custom reports
  • Perform peer review / QC of custom report programming
  • Create and implement database scripts to correct issues
  • Participate in departmental discussions regarding technical, functional and process improvement
  • Ensure that all project-related programming tasks are completed in accordance with standard practices throughout the lifecycle of the project including, but not limited to: Perform data integration configuration, programming, and documentation Process Data Clarification Forms (DCFs) Manage and program targeted rules Oversee data outputs for integrity and accuracy
  • Perform data integration configuration, programming, and documentation

• Process Data Clarification Forms (DCFs)

  • Manage and program targeted rules
  • Oversee data outputs for integrity and accuracy
  • Triage, research and provide solutions for identified data issues
  • Communicate progress and roadblocks on programming efforts to internal and external stakeholders
  • Assist junior staff to troubleshoot programming issues
  • Contribute to department knowledge share for common issues, standard processes, guides, etc.
  • Bachelor’s degree in computer science, software engineering, information technology, informatics, or closely related field (or equivalent experience)
  • 5+ years of experience as a software developer, database analyst/programmer, or clinical software tester
  • Experience with Snowflake
  • Experience building reports in SSRS, Tableau, or other reporting tools
  • 2+ years’ experience with programming in Microsoft SQL and/or MySQL
  • 3+ years of experience programming in SAS
  • 5+ years of experience with Clinical Data Management and clinical development technology solutions
  • Understanding of the clinical trial processes, including common data standards (CDISC) and Study Data Tabulation Model (SDTM)
  • Ability to manage competing priorities and can work in a dynamic environment
  • Comfortable writing and troubleshooting complex SQL queries that include PIVOT, Indexing, CTE’s, Subqueries, etc.

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