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ORIC Pharmaceuticals Inc. Tech Stack

Clinical-stage oncology company developing PRC2 and EGFR inhibitors

Biotechnology Research South San Francisco, California 51–200 employees Founded 2014 Public Company

ORIC is a clinical-stage biopharmaceutical company with two lead candidates in prostate and lung cancer indications. The hiring mix is heavily regulatory and quality-focused—VP and director roles in regulatory affairs, CMC, and quality dominate the recent openings—indicating a company preparing for regulatory submissions and eventual commercialization. Tech stack reflects typical pharma infrastructure (Veeva Vault for document/regulatory management, NetSuite for financial operations, SAS for data analysis), with active adoption of Veeva Vault signaling investment in compliance-ready systems.

Tech Stack 12 technologies

Core StackSAS NetSuite Expensify DocuSign Box HPLC LC-MS GCP Excel Coupa Navan Veeva Vault
AdoptingVeeva Vault

What ORIC Pharmaceuticals Inc. Is Building

Challenges

  • Launch readiness and life cycle management
  • Global safety regulation compliance
  • Timely regulatory submissions
  • Scalable compliant enterprise applications
  • Efficient regulatory pathway
  • Public company compliance
  • Compliance with 21 cfr part 11
  • Preparing for health authority inspections
  • Data discoverability and interoperability
  • Regulatory risk mitigation

Active Projects

  • Global regulatory strategy development
  • Rinzimetostat medical strategy
  • Safety management plan development
  • Application architecture design
  • Multi-year enterprise applications roadmap
  • Internal systems for regulatory submissions
  • Digital transformation of development systems
  • Gdpr compliance program
  • Regulatory submission strategy
  • Manufacturing change impact assessment

Hiring Activity

Accelerating15 roles · 8 in 30d

Department

Healthcare
3
Engineering
2
Research
2
Sales
2
IT
1
Legal
1
Ops
1
Quality
1

Seniority

Director
7
Senior
3
VP
3
Mid
1

Notable leadership hires: Regulatory Affairs VP, CMC Regulatory Affairs Director, Director Quality

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About ORIC Pharmaceuticals Inc.

ORIC Pharmaceuticals develops small-molecule cancer therapies targeting resistance mechanisms. The company is advancing two clinical programs: ORIC-944, a PRC2 inhibitor for prostate cancer, and enozertinib, an EGFR/HER2 exon 20 inhibitor for non-small-cell lung cancer. Founded in 2014 and publicly traded, ORIC operates from dual hubs in South San Francisco and San Diego, California, with a workforce of 51–200 employees. The company's project and pain-point landscape centers on regulatory pathway efficiency, manufacturing scale-up, global compliance (21 CFR Part 11, GDPR), and launch readiness—typical challenges for a clinical program approaching IND or commercial submission phases.

HeadquartersSouth San Francisco, California
Company Size51–200 employees
Founded2014
Hiring MarketsUnited States

Frequently Asked Questions

What is ORIC Pharmaceuticals' lead product?

ORIC has two clinical-stage candidates: ORIC-944, a PRC2 inhibitor for prostate cancer via the EED subunit, and enozertinib (ORIC-114), a brain-penetrant EGFR/HER2 exon 20 inhibitor for NSCLC.

What tech does ORIC Pharmaceuticals use?

ORIC uses Veeva Vault for regulatory and document management, NetSuite for financials, Coupa for procurement, SAS and LC-MS/HPLC for research, and GCP for cloud infrastructure. The company is actively adopting Veeva Vault.

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