Senior Director of Information Systems / Digital Systems Lead
Scorpion Therapeutics, Boston, Massachusetts, us, 02298
Role Summary
Vor Biopharma is seeking a Senior Director of Information Systems / Digital Systems Lead to design and deliver the company’s digital systems strategy as we prepare for global commercialization of telitacicept. This role will lead the implementation and ongoing management of regulated and enterprise systems that support Quality, Regulatory, CMC, Medical Affairs, and Commercial teams. The role partners closely with functional leaders to ensure digital tools, data, and integrations support compliance, scalability, and efficient operations across the business, and will lead a small team of IT professionals.
Responsibilities
Digital Systems Strategy & Delivery
Own and execute the digital systems roadmap aligned with commercialization and growth goals
Implement and scale SaaS platforms across Quality, Regulatory, CMC, Medical Affairs, and Commercial
Ensure systems are well integrated, user-friendly, and compliant
Regulated Systems & Compliance
Manage selection, validation, and lifecycle of GxP systems (QMS, RIM, LMS, eTMF, ERP, etc.)
Partner with QA to support 21 CFR Part 11 and GxP compliance
Establish governance for system changes and releases
Data, Reporting & Integrations
Support data governance, reporting, and dashboards across functions
Oversee integrations between enterprise systems and external partners (CROs, CMOs)
Ensure data integrity, security, and traceability
Medical Affairs & Commercial Enablement
Support digital capabilities for Medical Affairs and Commercial teams (e.g., Veeva, CRM, MLR)
Enable compliant data flows and insights to support launch readiness and field engagement
Vendor & Program Management
Manage vendors, contracts, and system budgets
Track risks, timelines, and value delivery for digital initiatives
Support audit readiness and inspection preparation
Qualifications
Bachelor’s or Master’s degree in Information Technology, Computer Science
10+ years of experience leading enterprise or digital transformation in biotech/pharma, with at least 5 years in commercial-readiness environments and 5 years leading a team
Deep understanding of regulated systems (GxP, SOX, CSV) and hands-on experience with platforms such as Veeva Vault (QMS, RIM, MedComms, CRM), SAP/Sage, Kivo, Benchling, LIMS/MES, and Tableau/Power BI
Proven success building cross-functional digital roadmaps across Quality, Regulatory, and Commercial domains
Strong vendor management, budget oversight, and stakeholder communication skills
Experience preparing systems and teams for FDA, EMA, and PMDA inspections
Education
Bachelor’s or Master’s degree in Information Technology, Computer Science
Skills
GxP, SOX, CSV
Veeva Vault (QMS, RIM, MedComms, CRM), SAP/Sage, Kivo, Benchling, LIMS/MES, Tableau/Power BI
Digital roadmaps across Quality, Regulatory, and Commercial
Vendor management, budget oversight, stakeholder communication
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Responsibilities
Digital Systems Strategy & Delivery
Own and execute the digital systems roadmap aligned with commercialization and growth goals
Implement and scale SaaS platforms across Quality, Regulatory, CMC, Medical Affairs, and Commercial
Ensure systems are well integrated, user-friendly, and compliant
Regulated Systems & Compliance
Manage selection, validation, and lifecycle of GxP systems (QMS, RIM, LMS, eTMF, ERP, etc.)
Partner with QA to support 21 CFR Part 11 and GxP compliance
Establish governance for system changes and releases
Data, Reporting & Integrations
Support data governance, reporting, and dashboards across functions
Oversee integrations between enterprise systems and external partners (CROs, CMOs)
Ensure data integrity, security, and traceability
Medical Affairs & Commercial Enablement
Support digital capabilities for Medical Affairs and Commercial teams (e.g., Veeva, CRM, MLR)
Enable compliant data flows and insights to support launch readiness and field engagement
Vendor & Program Management
Manage vendors, contracts, and system budgets
Track risks, timelines, and value delivery for digital initiatives
Support audit readiness and inspection preparation
Qualifications
Bachelor’s or Master’s degree in Information Technology, Computer Science
10+ years of experience leading enterprise or digital transformation in biotech/pharma, with at least 5 years in commercial-readiness environments and 5 years leading a team
Deep understanding of regulated systems (GxP, SOX, CSV) and hands-on experience with platforms such as Veeva Vault (QMS, RIM, MedComms, CRM), SAP/Sage, Kivo, Benchling, LIMS/MES, and Tableau/Power BI
Proven success building cross-functional digital roadmaps across Quality, Regulatory, and Commercial domains
Strong vendor management, budget oversight, and stakeholder communication skills
Experience preparing systems and teams for FDA, EMA, and PMDA inspections
Education
Bachelor’s or Master’s degree in Information Technology, Computer Science
Skills
GxP, SOX, CSV
Veeva Vault (QMS, RIM, MedComms, CRM), SAP/Sage, Kivo, Benchling, LIMS/MES, Tableau/Power BI
Digital roadmaps across Quality, Regulatory, and Commercial
Vendor management, budget oversight, stakeholder communication
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