EDC Technical Consultant

We are seeking a highly skilled and technically driven EDC Technical Consultant to support a mission-critical Electronic Data Capture (EDC) platform used in clinical research. This role is ideal for someone with deep experience in PL/SQL, data integration, and EDC system support, who can translate research requirements into scalable, compliant, and efficient technical solutions.

Key Responsibilities

• Design and implement technical solutions to enhance or replace legacy clinical data systems, including integration with platforms like Informatica and PL/SQL.
• Serve as a technical lead for EDC-related initiatives, ensuring SOP compliance, documentation accuracy, and effective resource planning.
• Build and maintain PL/SQL procedures, data migration scripts, and ETL workflows to support enterprise-scale clinical applications.
• Collaborate with research stakeholders and business analysts to translate clinical requirements into actionable technical specifications.
• Develop and support custom portals and APIs for EDC teams, including secure authentication and data exchange using Azure and RESTful services.
• Perform impact and gap analyses for system upgrades, ensuring seamless transitions and minimal disruption to ongoing trials.
• Support reporting needs and troubleshoot escalated data issues as a Level 3 support contact.

Required Skills & Experience

• 10+ years of experience in software engineering or technical consulting within clinical research environments.
• Strong hands-on experience with PL/SQL, Informatica, ETL development, and data migration.
• Proven experience supporting or integrating with EDC platforms (e.g., InForm, Medidata Rave, REDCap).
• Familiarity with Azure DevOps, CI/CD pipelines, and secure data architecture.
• Excellent problem-solving, documentation, and communication skills.
• Experience working in SOP-driven, regulated environments with a focus on data accuracy and compliance.

Preferred Qualifications

• Experience building portals or tools for EDC teams using modern frameworks (e.g., React, Node.js).
• Knowledge of regulatory submission standards and clinical trial workflows.
• Prior experience supporting oncology or other therapeutic area studies.