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New · posted Oct 31

Nurix Therapeutics · Biotechnology

Director, Drug Safety

  • Brisbane, CA
  • On-site
  • Full-time
  • Director
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EmploymentFull-time
DeadlineOpen until filled

The role

Join Nurix’s pharmacovigilance team to help ensure patient safety across our clinical pipeline of targeted protein degradation therapies. As Director, Drug Safety, you’ll lead aggregate safety analysis, benefit–risk assessments, and safety strategy for assigned programs — shaping how we evaluate risk and bring new medicines safely to patients. It’s a chance to influence critical safety decisions at the intersection of clinical medicine, data, and drug development.

Medical Safety Leadership

  • Serve as the medical safety lead for assigned products, providing clinical and pharmacovigilance expertise to safety strategy and activities
  • Lead aggregate safety data analysis for signal detection, signal evaluation, and risk characterization
  • Conduct medical review and interpretation of safety data, contributing to benefit–risk assessments
  • Monitor emerging safety signals and proactively address potential safety risks through appropriate internal and external communication

Regulatory and Safety Documentation

  • Oversee medical review of Individual Case Safety Reports (ICSRs)
  • Author and review regulatory safety documents, including Development Safety Update Reports (DSURs) and safety sections of INDs and regulatory briefing books
  • 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

Clinical Development Support

  • Provide clinical input into safety aspects of clinical trial protocols, informed consent forms, and investigator brochures
  • Collaborate with clinical development, regulatory affairs, medical affairs, and other stakeholders to ensure a consistent global safety strategy

Governance and Cross-Functional Collaboration

  • Serve on safety governance committees, supporting strategic decision-making for risk mitigation and benefit–risk evaluation

What you need

What You’ll Bring

  • 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
  • Experience supporting early clinical development and small biotechnology companies
  • Demonstrated expertise in aggregate safety analysis and benefit–risk evaluation
  • Strong knowledge of global pharmacovigilance regulations and guidance (ICH, FDA, EMA, MHRA)
  • Experience interacting with global health authorities on safety matters
  • Familiarity with signal detection and safety surveillance tools and databases
  • Strong communication, collaboration, and cross-functional leadership skills
  • 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

The posted range applies to roles based in the San Francisco Bay Area and reflects local market conditions. Where an offer lands within that range depends on the candidate’s relevant experience, technical expertise, and how their background aligns with the role’s requirements.

Pay

$247,300 – $317,100 a year

Employer provided
How this compares

Salary Range: Non-MD $247,300 - $280,400 | MD $295,000 - $317,100

Where you'll work

Brisbane, CAOn-siteOpen in Maps (opens in a new tab)

More jobs in Brisbane, CA
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From the posting

About Nurix

Fit with Nurix Culture and Values

  • Strong team orientation; highly collaborative
  • Solutions and results-oriented focus
  • Hands-on approach; resourceful and open to diverse points of view

About Nurix Therapeutics

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. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.

Nurix company page · 15 open roles

Job intelligence

The context around this role

Live data · October 31, 2026

Salary intelligence

How the pay compares

This role's midpoint is 9% above the US median for Clinical Safety & Pharmacovigilance roles at this level.

This roleEmployer provided

$247,300 to $317,100 a year

Director roles in California18 roles publishing pay

Middle half $227,125 to $280,750, median $254,250

Director roles in the US69 roles publishing pay

Middle half $213,500 to $281,000, median $260,000
Annual base pay
Annual base payLowMedianHigh
This role$247,300—$317,100
California$227,125$254,250$280,750
All US$213,500$260,000$281,000

This role: Nurix Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Safety & Pharmacovigilance

The general path across 113 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Nurix's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Associate, Pharmacovigilance Operations/Drug Safety · Clinical Sciences Partnership COE Coordinator

  2. Earlier

    Senior & Principal

    Often: Senior Safety Scientist · Clinical FSP Quality Manager

    $186K median11 open
  3. One step back

    Manager

    Often: Senior Manager, Clinical Quality Assurance · Clinical FSP Quality Manager

    $170K median15 open
  4. This role

    Director

    Often: Director · Senior Medical Director

    $260K median70 open
  5. Next step

    VP & Executive

    Often: Head of Multiple Myeloma & AML, Oncology · Head of Patient-Facing Quality Assurance

    $347K median12 open

Skills DNA

What this role leans on

How many of the posting's 24 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesDocumentation and SOPs: 2 linesInvestigations and CAPA: 1 lineRegulatory submissions: 1 lineQuality systems and risk: 3 linesClinical trial conduct: 4 linesCollaboration and leadership: 9 linesGMPDocumentationInvestigationsSubmissionsQuality systemsClinical trialsTeamwork
  • Collaboration and leadership9
  • Clinical trial conduct4
  • Quality systems and risk3
  • GMP and compliance2
  • Documentation and SOPs2
  • Investigations and CAPA1
  • Regulatory submissions1

Company hiring pulse

Nurix on Regulatory Jobs

15
Open roles
15
Distinct roles
1
Locations

By discipline

  • Regulatory5 33%
  • Quality5 33%
  • Clinical5 33%

By level

  • Director8 53%
  • Manager5 33%
  • Senior & Principal2 13%
See all 15 Nurix roles

More roles at Nurix

All 15 Nurix roles

Similar Clinical Safety & Pharmacovigilance roles elsewhere

Director, Drug Safety at Nurix

Open until filled. $247K–$317K a year, employer provided.

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