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Excelya

Oracle Programmer

Excelya

. Provide Oracle Programming input for Data Management activities dedicated to one Sponsor .

Posted 9/24/2026full-timeBengaluru • IndiaJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Oracle Programming, particularly with DMW and LSH tools, ensuring compliance with clinical programming standards and high-quality data management. Proficient in PL/SQL and JavaScript, with a solid understanding of clinical trial processes and relevant regulatory guidelines.

Highest-signal resume keywords
Oracle ProgrammingOracle DMW ToolPL/SQLJavaScriptICH GCP Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Oracle ProgrammingPL/SQLJavaScriptData ManagementSDTM ApplicationTransformation MappingExternal Data IntegrationVC/PD Programming
Tools & Technologies
Oracle DMWOracle LSHMS ProjectMicrosoft WordMicrosoft ExcelMicrosoft PowerPoint
Industry Keywords
Clinical Trial ProcessesICH GuidelinesEU GuidelinesFDA Guidelines

Tech Stack

Tools & technologies
JavaScriptOracleSQL

About the role

Key responsibilities & impact
  • Provide Oracle Programming input for Data Management activities dedicated to one Sponsor
  • Ensure all clinical programming aspects comply with Client SOPs and are delivered to high quality
  • Work closely with different study stakeholders internally
  • Program using Oracle tools including DMW and LSH
  • Apply SDTM and generate datasets according to DMW specifications
  • Set up external data vendor integrations from DMW specifications
  • Perform transformation mapping according to specifications
  • Manage external data loading and integrations in DMW
  • Perform VC/PD programming in DMW

Requirements

What you’ll need
  • 2 to 4 years of experience as an Oracle Programmer or equivalent combination of education, training, and experience
  • Good understanding of Oracle DMW tool and study build as per the specifications
  • Experience with programming languages such as PL/SQL and JavaScript
  • Knowledge and understanding of ICH GCP and other relevant ICH, EU, or FDA guidelines
  • Understanding of clinical trial processes and data management activities
  • Proficiency in office computer technologies including Word, Excel, PowerPoint, and MS Project
  • Fluency in English

Benefits

Comp & perks
  • Equal opportunities for all
  • Diverse, equitable, and inclusive workplace
  • Opportunities to evolve through diverse projects
  • Opportunity to work alongside preeminent experts
  • Professional and intellectual growth
  • Stimulating professional environment
  • Employee community centered on care, collaboration, and purpose