IT Business Partner, R&D and Compliance (Remote)

Description The IT Business Partner, R&D and Compliance serves as the strategic and operational bridge between R&D functions and IT, with particular ownership of the Veeva R&D application landscape (QMS, RIM, and related modules). This role translates R&D business needs and regulatory compliance into technology roadmaps and continuous improvement. One main focus is to ensure IT delivery is compliant, scalable, and aligned with global R&D and enterprise strategy. This position reports to the Chief Financial Officer. This is a remote-based position located in the United States. Responsibilities: Act as the primary IT partner for designated R&D functions (e.g., Regulatory Affairs, Quality, Clinical Development), building and maintaining an account/relationship planOwn the strategy, roadmap, and lifecyle for Veeva R&D systems - including Veeva Vault QMS (quality management, deviations, CAPA, change control) and Veeva Vault RIM (regulatory information management, submissions, registrations)Translate business and regulatory priorities into actionable technology plans, providing effort estimates and prioritization within IT investment cyclesLead or oversee system configuration, validation, and change control activities for Veeva platforms in a GxP-regulated environmentPartner with Quality and Regulatory stakeholders to ensure Veeva systems support evolving compliance requirements (21 CFR Part 11, GxP, global submission standards)Build business cases for platform enhancements, integrations, and new capabilities; manage associated budgetsCoordinate with enterprise architecture, data, and security teams to ensure Veeva and adjacent R&D systems are integrated and "global by design"Manage relationships with Veeva and other third-party vendors/implementation partnersCommunicate project status, risks, and escalations to IT and R&D leadershipMentor junior IT business partners or analysts supporting the Veeva platform portfolioIdentify opportunities for automation, AI/ML, or process improvement within QMS/RIM workflows Requirements Bachelor's degree in IT, Life Sciences, or related field8 years in a client-facing IT role within pharma/biotech, with increasing responsibilityHands-on experience with Veeva Vault QMS and Veeva Vault RIM (configuration, validation, or business ownership - specify which your org needs)Strong understanding of GxP-regulated environments, computer system validation (CSV/CSA), and change control processesExperience with regulatory submission processes and/or quality management processes in pharma R&DProven ability to translate business/regulatory needs into technical requirements and delivery plansStrong stakeholder management and communication skills across technical, scientific, and regulatory audiencesExperience building business cases and managing project or platform budgetsExperience managing regulatory compliance globally Veeva-specific certifications (e.g., Veeva Vault QMS or RIM Administrator) a plusPost-market compliance experience a plusAbility to demonstrate Elevar’s core values by holding ourselves and each other accountable for the work we do, taking time to collaborate effectively while working remotely, making space for ingenuity in work and thought, and staying grounded in compassion The anticipated annual base salary range for this role is $120,000 to $150,000. Final compensation depends on multiple factors including but not limited to, relevant experience, skillset, depth and breadth of knowledge, internal equity, and external market factors. Elevar Therapeutics is a rapidly growing biotech company that offers competitive wages and benefits package including medical, dental, vision, time off, a retirement plan, and other voluntary benefits for employees.