Full-Time

Director IT Business Partner

Commercial

Alumis

Alumis

201-500 employees

Develops precision therapies for immune diseases

No salary listed

San Bruno, CA, USA

Hybrid

On-site Tuesday-Thursday required; remote applicants may be considered case-by-case.

Bachelor's, Master's, PhD

Category
IT & Security (1)
Required Skills
Veeva
SAP Products
Salesforce

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Requirements
  • Bachelor's degree in Information Technology, Computer Science, Life Sciences, or a related field; advanced degree preferred.
  • 10+ years of IT experience, with at least 5 years in a business partner, IT lead, or equivalent role supporting commercial functions in biotech or pharma.
  • Demonstrated experience supporting pre-commercial or launch-stage activities at a small to mid-sized life sciences company.
  • Deep expertise with commercial systems such as Veeva CRM, Salesforce, SAP, or equivalent platforms.
  • Strong understanding of pharmaceutical commercial operations, including field force, commercial strategy, marketing, market access, and medical affairs.
  • Hands-on experience delivering IT solutions across Commercial Strategy, Marketing Technology, Market Access, and Medical Affairs functions, with a clear understanding of the business workflows and data needs unique to each.
  • Proven ability to manage multiple concurrent initiatives in a fast-paced, resource-constrained environment.
  • Proven track record of managing and developing direct reports, including setting goals, providing coaching, and building high-performing teams in a dynamic environment.
  • Experience managing external vendors, system integrators, and managed service providers — including contract negotiation, performance management, and holding partners accountable to delivery commitments and SLAs.
Responsibilities
  • Own the IT strategy and roadmap for commercial-facing systems, including CRM (e.g., Veeva, Salesforce), ERP, contract management, and master data management (MDM) platforms.
  • Lead end-to-end delivery of commercial technology initiatives — from requirements gathering and vendor selection through implementation, validation, and go-live.
  • Ensure systems are configured to support pre-commercial activities such as field force deployment, sample management, HCP/HCO data management, and promotional materials tracking.
  • Serve as the primary IT liaison for Commercial, Market Access, Marketing, and Sales Operations stakeholders.
  • Partner with business leaders to identify technology gaps, define requirements, and prioritize the IT portfolio in alignment with launch timelines and commercial goals.
  • Translate complex technical concepts into clear business value for non-technical audiences.
  • Partner with commercial leadership to shape the long-term IT strategy that enables go-to-market planning, competitive positioning, and portfolio decision-making.
  • Support business intelligence and reporting capabilities that provide insights into market trends, sales performance, and customer engagement.
  • Oversee IT solutions supporting multichannel marketing execution, including digital engagement platforms, content management systems (CMS), and marketing automation tools.
  • Ensure integration between marketing platforms and CRM systems to enable coordinated customer engagement across channels.
  • Support technology solutions for payer and account management, including contract management, formulary tracking, and gross-to-net analytics platforms.
  • Partner with Market Access stakeholders to ensure data flows and reporting capabilities support reimbursement strategy and pull-through activities.
  • Enable IT solutions for Medical Affairs functions, including medical information platforms, KOL engagement tracking, scientific exchange tools, and congress/event management.
  • Ensure Medical Affairs systems meet compliance and regulatory requirements for appropriate off-label and on-label scientific communication.
  • Drive IT readiness activities in support of product launch, including system build-out, user acceptance testing (UAT), training, and hypercare support.
  • Collaborate cross-functionally with Regulatory, Legal, Compliance, and Finance to ensure commercial systems meet applicable requirements (e.g., PDMA, OIG guidelines, data privacy regulations).
  • Lead, mentor, and develop a team of IT professionals supporting commercial functions, fostering a culture of accountability, collaboration, and continuous improvement.
  • Define roles, responsibilities, and performance expectations; support career development and succession planning within the team.
  • Manage relationships with third-party vendors, system integrators, and managed service providers supporting commercial technology.
  • Negotiate contracts and SLAs; hold vendors accountable to delivery commitments and quality standards.
  • Ensure commercial systems adhere to IT governance, data integrity, and security standards.
Desired Qualifications
  • Experience supporting the commercial launch of one or more pharmaceutical or biologic products.
  • Familiarity with specialty pharma or rare disease commercial models.
  • Knowledge of data privacy regulations (HIPAA, GDPR) and industry compliance standards (PDMA, OIG).
  • Experience with master data management (MDM) and data governance in a commercial context.
  • Familiarity with commercial analytics tools (e.g., IQVIA, Symphony Health data integrations, Tableau, Power BI).
  • PMP, ITIL, or equivalent certification.

Alumis develops precision therapies for immune-mediated diseases. By using genetic and disease biology insights, it designs targeted treatments and selects the right targets, molecules, indications, patient groups, endpoints, and possible combinations to optimize outcomes. The company differentiates itself by aligning therapy development with genetic and immunologic understanding to match medicines to the patients who will benefit most. Its goal is to improve clinical outcomes by bringing precision therapies to market and pursuing partnerships or licensing to support development and commercialization.

Company Size

201-500

Company Stage

IPO

Headquarters

South San Francisco, California

Founded

2021

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Simplify Jobs

Simplify's Take

What believers are saying

  • August 13, 2026 results kept the envudeucitinib psoriasis NDA on track for Q4 2026.
  • Deep Track Capital bought 6.77 million shares in Q1 2026, validating the pipeline.
  • June 30, 2026 cash reached $502.3 million, funding operations into Q4 2027.

What critics are saying

  • Q2 2026 revenue fell to $1.7 million while net loss widened to $142.2 million.
  • Lonigutamab impairment and strategic review signal damaged asset value after the ACELYRIN merger.
  • Single-asset dependence on envudeucitinib makes a Q4 2026 NDA failure existential.

What makes Alumis unique

  • Envudeucitinib combines TYK2 inhibition with late-stage psoriasis and lupus programs in 2026.
  • Alumis pairs oral immunology assets with CNS-penetrant A-005 for Parkinson's and multiple sclerosis.
  • The 2025 ACELYRIN merger created a broader immune-mediated diseases platform under one management team.

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Benefits

Health Insurance

Unlimited Paid Time Off

Remote Work Options

Commuter Benefits

Phone/Internet Stipend

Gym Membership

Stock Options

Performance Bonus

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

4%
Associated Press
Aug 13th, 2026
Alumis' envudeucitinib achieves 54% complete skin clearance in psoriasis trial, NDA submission planned Q4 2026

Alumis reported second quarter 2026 financial results, highlighting that 54% of patients achieved complete skin clearance in its ONWARD3 trial for envudeucitinib in plaque psoriasis after 48 weeks. The company remains on track to submit a New Drug Application to the FDA for the treatment in Q4 2026. The biopharmaceutical firm anticipates potentially pivotal Phase 2b LUMUS topline data for envudeucitinib in systemic lupus erythematosus in Q3 2026. Alumis plans to initiate a Phase 2 biomarker trial for A-005, its CNS-penetrant TYK2 inhibitor, in Parkinson's disease patients in the first half of 2027. As of 30 June 2026, Alumis held cash, cash equivalents and marketable securities of $502.3 million. Research and development expenses decreased to $85.3 million from $108.8 million year-over-year. Net loss was $142.2 million for the quarter.

Intellectia AI
May 25th, 2026
Deep Track Capital Acquires Significant Stake in Alumis

- **Stake Acquisition**: Deep Track Capital disclosed a purchase of 6,772,595 shares of Alumis in Q1 2026, valued at approximately $169.31 million, in...

Yahoo Finance
May 24th, 2026
Deep Track Capital invests $169M in biotech Alumis, up 355% on TYK2 drug pipeline

Deep Track Capital acquired 6,772,595 shares of Alumis (NASDAQ:ALMS) during the first quarter of 2026, an estimated $169.31 million investment based on quarterly average pricing, according to a 15 May SEC filing. The biotechnology company develops therapies for autoimmune and neuroinflammatory diseases. Its lead candidate, envudeucitinib, showed strong Phase 3 psoriasis results with PASI 90 response rates of 68.0% and 62.1% by Week 24. Alumis plans to submit an NDA in the fourth quarter, whilst pivotal Phase 2b lupus data are expected in the third quarter. Alumis shares were trading at $22.02, up 355% over the past year, outperforming the S&P 500's 28% gain. The company held $569.5 million in cash as of quarter-end, sufficient to fund operations into the fourth quarter of 2027.

Yahoo Finance
May 15th, 2026
Major healthcare investor cuts Alumis stake by $10.3M despite stock's 327% surge

Omega Fund Management sold 411,968 shares of Alumis in the first quarter, reducing its stake to 241,255 shares, according to an SEC filing. The transaction was valued at approximately $10.3 million based on quarterly average pricing. Despite the sale, Alumis remains a meaningful holding for Omega at 3.3% of assets under management. The move appears to be profit-taking following Alumis shares' 327% gain over the past year, significantly outperforming the S&P 500's roughly 25% increase. Alumis, a clinical-stage biotechnology company developing therapies for autoimmune diseases, recently reported positive late-stage psoriasis data for its lead TYK2 inhibitor candidate. The company plans an FDA submission in the fourth quarter and ended the quarter with $569.5 million in cash, sufficient to fund operations into late 2027.

Yahoo Finance
May 10th, 2026
ACT Capital's $4M Alumis stake eyes TYK2 inhibitor with 65% psoriasis clearance rate

ACT Capital Management has acquired 174,250 shares of Alumis for approximately $4.36 million, establishing a new position representing 3.02% of its assets under management, according to an SEC filing dated 8 May 2026. The clinical-stage biotechnology company focuses on autoimmune and neuroinflammatory disorders, with lead candidates targeting TYK2 inhibition. Alumis shares have surged 350% over the past year to $23.76, driven by positive Phase 3 data showing 65% of patients achieving PASI 90 skin clearance in plaque psoriasis trials. The company plans to submit a new drug application in the second half of 2026 and expects pivotal Phase 2b lupus data in the third quarter. Alumis raised $345 million in January and held $308.5 million in cash at year-end, despite posting a $243 million net loss.