Nurix Therapeutics

Nurix Therapeutics

Director, Drug Safety

Brisbane, California · Director

Sponsorship not specified$247k-$280kDetected 10 days ago
Data AnalysisPatient CareFDA RegulatoryPharmacovigilanceLeadershipCommunicationCollaborationRegulatory Affairs

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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

  • Conduct medical review and interpretation of safety data, contributing to benefit-risk assessments
  • Oversee medical review of Individual Case Safety Reports (ICSRs)

Responsibilities

  • Clinical Development Support
  • Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases.

Requirements

  • Strong knowledge of global pharmacovigilance regulations and guidance (ICH, FDA, EMA, MHRA)
  • Familiarity with signal detection and safety surveillance tools and databases
  • Ability to interpret complex clinical and safety data and translate insights into regulatory and business strategy
  • Ability to work effectively and collaboratively in a fast-paced, growing organization across functional boundaries

Nice to have

  • Monitor emerging safety signals and proactively address potential safety risks through appropriate internal and external communication
  • Contribute to safety responses to regulatory authorities and participate in regulatory interactions
  • Provide clinical leadership during inspections and audits related to safety and risk management
  • Provide clinical input into safety aspects of clinical trial protocols, informed consent forms, and investigator brochures
  • Advanced clinical or scientific degree, such as MD, DO, PharmD, or equivalent relevant training and experience
  • Clinical experience preferred
  • 5-10 years of experience in pharmacovigilance/drug safety within the pharmaceutical or biotechnology industry

Skills

  • Strong communication, collaboration, and cross-functional leadership skills

Compensation

  • Non-MD $247,300 - $280,400 | MD $295,000 - $317,100

Benefits

  • Collaborate with clinical development, regulatory affairs, medical affairs, and other stakeholders to ensure a consistent global safety strategy

This listing is sourced directly from Nurix Therapeutics's careers page and normalized into a canonical job model.