Nurix Therapeutics

Nurix Therapeutics

Director, Nonclinical Toxicology Operations

Brisbane, California, United States · Director

Sponsorship not specified$221k-$253kDetected 17 days ago
Project ManagementLogisticsVendor ManagementProcurementPharmacologyPatient CarePharmacovigilanceResearchAnimal StudiesLeadershipCommunicationOrganizational Skills

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odds of building a lasting career here

59Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds (Level IV)94
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~61% per draw at Level IV). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

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Employer immigration record

from this employer's Department of Labor filings

Files H-1B transfers

2 transfer filings in the last year, covering 2 workers. Median labor-condition decision: 8 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • The role will be responsible for operations activities including owning timelines, budgets, contracts, and cross-functional coordination for a portfolio of targeted protein degradation programs.
  • You will thrive here if you are highly organized, scientifically fluent, comfortable holding teams and stakeholders to a schedule, and energized by turning complex, interdependent work into clear milestones and decisions.

Responsibilities

  • Toxicology study support and vendor management
  • Partner with Toxicology Leads and Study Directors to scope, design, and schedule GLP and non-GLP in vivo and in vitro safety studies, including exploratory tox, DRF, GLP repeat-dose toxicology, safety pharmacology, and genetic toxicology.
  • Identify, qualify, and manage CROs and specialty vendors
  • Own the contract lifecycle: draft and route work orders, MSAs, change orders, and amendments
  • reconcile invoices and support accruals and forecasting.
  • Build and maintain integrated study timelines
  • Coordinate protocol and report review cycles, ensuring documents move efficiently through internal review, QA, and sign-off.
  • Program management, late lead optimization to IND
  • Serve as project manager for assigned discovery and development programs from late lead optimization through candidate selection, IND-enabling studies, and IND filing.

Requirements

  • Required: M.S. or Ph.D. in a life sciences discipline (toxicology, pharmacology, biology, chemistry, pharmaceutical sciences, or related).
  • Track deliverables required for regulatory submissions, including study reports, certificates of analysis, and test article documentation.
  • Education
  • Preferred: formal project management credential such as PMP.
  • Experience
  • Skills and attributes
  • Proficiency with project management tools and methods, including integrated timelines, critical path analysis, and resource planning (e.g., MS Project, Smartsheet, Planisware, or equivalent). Familiarity with AI tools a plus.

Nice to have

  • Typically, 10+ years of relevant biotech or pharmaceutical experience, including demonstrable project management ownership of multidisciplinary programs.
  • Track record managing CROs and external vendors, including contracting, budget tracking, and performance management.
  • Direct experience supporting and coordinating IND-enabling activities
  • Working knowledge of small molecule drug discovery and development, nonclinical safety assessment, and GLP requirements, with scientific fluency sufficient to plan, question, and integrate the work.
  • Experience in targeted protein degradation, oncology, or immunology is an advantage.
  • Proficiency with project management tools and methods, including integrated timelines, critical path analysis, and resource planning (e.g., MS Project, Smartsheet, Planisware, or equivalent).
  • Familiarity with AI tools a plus.
  • Clear, concise written and verbal communication

Skills

  • Exceptional organizational skills and attention to detail, with the judgment to know what matters and what does not.
  • Clear, concise written and verbal communication; able to present status and risk to senior leadership without embellishment.
  • Comfort with ambiguity and shifting priorities in a fast-moving discovery environment.
  • Strong team orientation; highly collaborative
  • Solutions and results-oriented focus
  • Hands-on approach; resourceful and open to diverse points of view
  • Act as a connective hub across functions and sites, resolving interface issues before they become timeline issues.
  • Contribute to continuous improvement of project management practices, templates, and tools within the group.

Compensation

  • $220,700 - $252,667
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