Technical Project Manager

About the role

The Technical Project Manager leads end‑to‑end delivery of technical components for clinical trials within a drug or vaccine program. You will design, build, test, deploy and maintain study‑level technical deliverables while ensuring compliance with clinical data standards and GxP requirements.

Key responsibilities

• Develop and maintain detailed project plans covering design, build, testing, deployment, run and close‑out of technical deliverables such as eCRFs, data‑collection systems, integrations, edit checks, listings, reports and archival.
• Lead discovery sessions with study stakeholders to define technical requirements, assess complexity and set timelines.
• Ensure consistent use of clinical database standards and manage change‑request intake and processing.
• Orchestrate configuration and build activities with full traceability to requirements, providing status reporting and governance updates.
• Tri­age defects, manage change requests, and maintain audit‑ready documentation throughout the study lifecycle.
• Serve as the primary technical point of contact for the trial, representing Global Clinical Data Integration on cross‑functional teams.
• Validate that all technical components are production‑ready before first‑patient‑first‑visit and support end‑of‑study archival and decommissioning.
• Support audits and inspections, ensuring validation evidence meets SOP/GxP expectations.

Required profile

• Bachelor’s degree (field not specified).

Required skills

• Clinical database standards
• GxP compliance
• eCRF design and configuration
• Data‑collection system implementation
• System integration
• Edit checks and derivations
• Validation and audit‑ready documentation