Director, Digital Technology Lead - Clinical and Development

Join Us in Tackling Autoimmune Disease at Its Root

At Vor, we believe science can do more than manage symptoms. It can change the course of disease. By advancing telitacicept, a first- and potentially best-in-class dual BAFF/APRIL inhibitor, we are silencing upstream survival signals and stopping downstream autoimmune cascades. Together, we are addressing disease at its root cause and rewriting what is possible for patients worldwide.

When you join Vor, you’re not just working on a medicine. You’re part of a mission to redefine the future of autoimmune care.

Why Work at Vor?

Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases.

Growth: Be part of a rapidly scaling company with opportunities to grow your career in science, clinical development, commercial strategy, and beyond.

Innovation: Work on a platform with potential beyond one indication — a therapy that has already shown consistent results across lupus, IgA nephropathy, and Sjögren’s syndrome.

Belonging: Join a culture where every voice is heard, and where our shared mission unites us across functions and geographies.

 

 

The Digital, Data, and Technology (DD&T) organization seeks a strategic and technically proficient leader to act as the primary liaison between Information Technology and the Clinical & Development organization—which includes Clinical Operations, Clinical Development, Biometrics, Regulatory, and related functions. This director-level role, reporting to the Head of Digital, Data, and Technology, is responsible for shaping the organization's digital roadmap, aligning scientific and operational objectives with technology strategy and implementation, and ensuring delivery of secure, compliant, and scalable solutions that advance medicine development. The Director will collaborate closely with business leadership, Product and Platform teams, Enterprise Architecture, Cybersecurity, Data and AI, Quality, and external vendors to drive tangible business results.

Key Responsibilities

· Strategic partnership & demand shaping: Build trusted relationships with R&D leaders; proactively identify opportunities where digital capabilities improve cycle time, cost, quality, and scientific insight; shape and prioritize demand into an outcome-based portfolio.

· R&D digital roadmap: Co-create and maintain a multi-year technology roadmap aligned to enterprise strategy, data strategy, and target architecture; balance innovation with standardization and technical debt reduction.

· End-to-end delivery accountability: Oversee delivery of technology initiatives (e.g., ELN/LIMS, SDMS, CTMS/eTMF, clinical data platforms, safety systems, regulatory submissions, R&D analytics); ensure adoption, change management, and benefit realization.

· Data, digital, and AI enablement: Drive the delivery of AI-powered solutions that improve efficiency, reduce cycle times, and enhance scientific and operational decision-making. Define a data strategy for managing the flow of data from site to submission in are integrated and traceable manner.

· GxP compliance & quality: Ensure R&D digital solutions are delivered and operated in compliance with applicable GxP regulations and company Quality Management System requirements, including CSV/validation practices, data integrity, audit trails and e-signatures (e.g., 21 CFR Part 11/Annex 11), vendor oversight, and inspection/audit readiness.

· Operating model leadership: Drive effective ways of working across Business, DD&T and Product teams (Agile/Lean practices, product lifecycle management, DevSecOps where applicable); clarify roles, decision rights, and SLAs.

Required Qualifications

· Bachelor’s degree in Information Systems, Computer Science, Engineering, Life Sciences, or a related field (or equivalent experience).

· 10+ years of progressive experience in IT, digital, product, or technology leadership with significant engagement in R&D within pharma/biotech/medical devices or closely related regulated industries.

· Demonstrated experience partnering with senior R&D stakeholders (e.g., VP/SVP level) to define strategy, influence priorities, and deliver measurable outcomes.

· Strong understanding of the R&D value chain (discovery to development), scientific data types, and key R&D systems and platforms.

· Experience implementing key R&D applications such as ELN, LIMS, SDMS, CTMS, eTMF, EDC, pharmacovigilance/safety, regulatory information management, and/or lab automation connectivity.

· Proven knowledge of regulated computerized system lifecycle practices, including validation/CSV, data integrity, and audit r