ORIC Pharmaceuticals Inc. · 1 month ago
Director Information Technology, Development Operations
12265 El Camino Real, San Diego, CA 92130, USA
Full-time
Onsite
Director/Executive
$200K/yr - $250K/yr
8+ years expORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives by Overcoming Resistance In Cancer. The Director of Information Technology, Development Operations will support late-stage Development functions across Clinical, Regulatory, Quality, and Drug Safety, driving digital enablement and compliance for Phase 3 programs.
BiopharmaBiotechnologyHealth CarePharmaceuticalTherapeutics
Responsibilities
Serve as the primary IT partner for Phase 3 Development functions, aligning technology solutions with business needs
Collaborate with Clinical, Safety, Regulatory, Portfolio & Project Management, and other Development functions and teams to support digital transformation initiatives
Lead implementation and optimization of Veeva Vault applications (e.g., Quality Docs, QMS, RIMS)
Gather application business requirements and systems goals from business owners and translate them into technical requirements
Oversee system lifecycle management, including upgrades, integrations, and vendor coordination for SAS, Box.com, and Extedo
Collaborate with domain leaders, governance, and platform teams to ensure seamless integration of Development systems
Ensure systems are validated per GxP requirements and compliant with 21 CFR Part 11
Lead the IT GDPR compliance program
Own CSV documentation and audit readiness for IT-supported platforms
Partner with QA and Regulatory to prepare for health authority inspections
Provide IT support during inspections, including system demonstrations and documentation
Lead cross-functional projects from concept through deployment
Manage change control processes and ensure stakeholder alignment
Manage the UAT planning, execution, and reporting
Qualification
Required
Bachelor's or Master's degree in Computer Science, Life Sciences, or related field
8+ years of experience in IT supporting development functions in the biopharma industry
Strong knowledge of Veeva Vault applications and their configuration
Proven experience with CSV, GxP systems, and 21 CFR Part 11 compliance
Familiarity with Phase 3 clinical trial operations and regulatory submission processes
Good understanding of industry data standards (CDISC, MedDRA, HL7, etc.)
Experience in R&D data domains and lifecycle
Excellent communication, stakeholder management, and problem-solving skills
Preferred
Experience supporting global clinical trials and regulatory submissions
Prior involvement in inspection readiness or direct participation in regulatory audits
Knowledge of Quality Management Systems (QMS)
Company
ORIC Pharmaceuticals Inc.
ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives by Overcoming Resistance In Cancer.
51-200 employees
H1B Sponsorship
ORIC Pharmaceuticals Inc. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2024 (1)
2022 (3)
2021 (3)
2020 (1)
Funding
Current Stage
Public CompanyTotal Funding
$533MKey Investors
SR OneNextech InvestPfizer
2025-05-28Post Ipo Equity· $125M
2024-01-30Post Ipo Equity· $125M
2023-06-26Post Ipo Equity· $85M
Leadership Team
Jacob Chacko
CEO
Dominic Piscitelli
Chief Financial Officer
Recent News
2025-12-24
2025-12-18
2025-12-18
Company data provided by crunchbase