Nurix Therapeutics

Nurix Therapeutics

Clinical Trial Manager (CTM)

Brisbane, California · Senior

Sponsorship not specified$158k-$168kDetected 17 days ago
GCPForecastingPatient CareFDA RegulatoryProblem SolvingOrganizational Skills

Stay score

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.

Personalize to your clock →

H-1B wage level

the lottery is wage-weighted — each level is one more entry

Level I · 1×
Level I$167,6481 entry
Level II$208,5822 entries
Level III$249,5383 entries
Level IV$290,4724 entries

The bottom of this range ($157,700) is below the Level I prevailing wage of $167,648. An H-1B cannot be filed below the prevailing wage, so an offer at the floor of this band could not be sponsored as posted.

DOL prevailing wage, 2026-27 wage year · Natural Sciences Managers (11-9121) · San Francisco-Oakland-Fremont, CA. Wage level is derived by USCIS from the offered wage, occupation and worksite; the occupation shown is inferred from the job title.

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.

Community outcomes

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About the role

  • Track trial progress and keep stakeholders updated on status
  • Monitor enrollment and address recruitment challenges as they arise
  • Draft and coordinate review of protocols, informed consents, CRFs, monitoring plans, and study reports

Responsibilities

  • Own all operational aspects of your assigned clinical trial(s)
  • Manage day-to-day CRO/vendor relationships to keep deliverables on budget, timeline, and protocol
  • Build strong working relationships with site investigators and study coordinators
  • Manage study budget, forecasting, accruals, and vendor payments for your trial(s)
  • Partner with Data Management on CRF content, completion guidelines, and data deliverables
  • Prepare for and support regulatory agency audits and inspections
  • 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.
  • Clear, confident communicator who can create direction for a study team

Requirements

  • Ability to travel as required for the program (25%)
  • Working knowledge of FDA, EMA, ICH, and GCP regulations and guidelines

Skills

  • Strong analytical and problem-solving skills

Compensation

  • $157,700 - $168,200 annually

Company info

  • Thrives in a fast-paced, small-company environment

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