> Markdown version of [/jobs/ext/4633137-lead-software-engineer](https://www.wearedevelopers.com/jobs/ext/4633137-lead-software-engineer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Lead Software Engineer - **Company:** Virtusa Corporation - **Location:** Indianapolis, IN, United States - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Cerner, Agile Methodology, Clinical Data Management, Clinical Data Repository, Electronic Data Capture, Oracle (Applications), Software Engineering, Verification and Validation (Software), EHR Systems, Electronic Medical Records, Veeva, VeevaVault - **Published:** November 8, 2026 - **Apply:** https://www.careerbuilder.com/job-details/lead-software-engineer-indianapolis-in--e53c8c4a-0313-470d-905e-5794ec28e396 ## About the Role Software Engineering, eSourcing, Technical Delivery, Clinical Data Management, Electronic Medical Records, Clinical Trial, Data Collection, Regulatory Requirements, Data Quality, Electronic Data Capture (EDC), eSource & Clinical Data Platforms: Deep knowledge and hands-on technical experience with EDC systems (e.g., Oracle InForm, Veeva Vault EDC/CDMS), EMR/EHR platforms (e.g., Epic, Oracle Health), and DDC solutions (e.g., Veeva Vault eSource, TrialKit, ClinCapture). Validation & Compliance: Hands-on experience in verification, validation, and software lifecycle compliance within regulated clinical/pharma environments. Agile Backlog Management: Proven ability to manage product backlogs, prioritize feature enhancements, and lead cross-functional requirement sessions. Vendor & Stakeholder Management: Excellent collaboration skills to interface effectively between business owners, technical engineering teams, and third-party technology providers. ## Description The eSource Technical Subject Matter Expert (SME) is responsible for delivering technical expertise for eSource systems (Electronic Medical Records / Direct Data Capture) to support eData capture initiatives, drive efficient and compliant clinical trial operations, and ensure high-quality data deliverables. The SME serves as the central technical authority aligning system capabilities, clinical data management needs, regulatory requirements, and vendor delivery. eSource Technical Ownership: Serve as the primary Technical Subject Matter Expert (SME) for eSource, Electronic Medical Records (EMR), Direct Data Capture (DDC), and Electronic Data Capture (EDC) platforms such as Medidata/ Veeva EDC Verification & Validation: Oversee end-to-end verification and validation of third-party vendor capabilities and eSource/EMR integration solutions, ensuring strict alignment with quality, regulatory, and technical standards. Compliance & Standards Alignment: Conduct technical evaluations of vendor deliverables and clinical data capture tools to ensure adherence to corporate standards and clinical processes. Backlog & Feature Prioritization: Manage and prioritize the product backlog for eSource system enhancements, serving as the central liaison between business stakeholders and external technology vendors. System Maintenance: Manage post-production technical support, post-go-live changes, and structural updates to ensure continuous system operational readiness. Cross-Functional & Vendor Liaison: Act as the primary technical bridge between business owners, clinical data management teams, and third-party vendors.