Senior EDC Developer

Senior EDC Developer (Remote)

Remote (U.S.) 6+ Months Contract C2C GC, USC

Senior EDC Developer with hands-on experience in EDC platforms (RAVE/Medrio/Zelta/Castor), SQL Server, Azure (DB/Blob), Power BI, MongoDB, and API integrations (JSON/XML).

Responsibilities

• Design, build, and implement EDC studies end-to-end using platforms like RAVE, Medrio, Zelta, or Castor

• Develop and maintain Azure DB and Blob storage , including database creation, cloning, and pipeline support

• Write and optimize SQL queries, stored procedures, and data validation logic in SQL Server

• Support MongoDB metadata structures for logging, configuration, and system operations

• Develop and maintain Power BI dashboards and reports for data insights and visualization

• Manage and support API integrations (JSON/XML) between EDC systems and external platforms

• Work with IIS, Windows Server, and Azure hosting environments for deployment and support

• Troubleshoot data, integration, and application issues to ensure system performance and accuracy

• Collaborate with cross-functional teams to understand study requirements and data workflows

• Required

• 2+ years of hands-on experience in EDC development (RAVE, Medrio, Zelta, Castor, etc.)

• Strong experience with SQL Server (queries, stored procedures, data validation)

• Experience with Azure services (DB, Blob Storage, pipelines)

• Familiarity with MongoDB for metadata/configuration support

• Experience in Power BI report development

• Solid understanding of APIs, JSON, XML, and system integrations

• Knowledge of IIS, Windows Server, and Azure hosting

• Strong analytical, troubleshooting, and problem-solving skills

• Excellent communication and ability to work independently

• Preferred

• Bachelor's or Associate's degree in Computer Science or related field

• Relevant certifications in Azure, SQL, or data platforms

• Experience with clinical data reconciliation processes

• Exposure to life sciences or clinical trial environments

• Nice to Have

• Experience working in regulated environments (GxP, clinical trials)

• Familiarity with data pipelines and ETL processes