- B2B
- Public StagePublicly traded company
- Top InvestorsThis company has received a significant amount of investment from top investors
In office
Not Available
About the job
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.
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.
About the company
- B2B
- Public StagePublicly traded company
- Top InvestorsThis company has received a significant amount of investment from top investors
