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.