Senior Clinical Trial Manager (Sr. CTM) NX-5948-203

Nurix Therapeutics

Brisbane (CA)

On-site

USD 140,000 - 190,000

Full time

14 days+

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Job summary

Scorpion Therapeutics is seeking a Senior Clinical Trial Manager to oversee multiple trials or regions, driving strategic operational planning, vendor management, and program-level oversight. You will shape protocol and study design, lead vendor/CRO selection and negotiation, manage budgets and financial risk, mentor junior staff, and ensure audit readiness, with on-site Brisbane, CA work and 25% travel.

This role requires deep regulatory knowledge and the ability to navigate complex global

Qualifications

  • 8-10+ years of industry experience in clinical operations.
  • Deep knowledge of FDA, EMA, ICH and GCP regulations.
  • Experience managing global/multi-region trials and vendor relationships at a strategic level.

Responsibilities

  • Represent Clinical Operations externally and internally.
  • Proactively identify and mitigate risks.
  • Lead cross-functional initiatives.
  • Shape protocol and study design.
  • Lead vendor/CRO selection and negotiation.
  • Manage budgets and financial risk.
  • Mentor junior staff and ensure audit readiness.

Skills

Mentoring
Influencing without authority
Organizational excellence
Adaptability

Education

BS in Biological Sciences

Job description

Role

Senior Clinical Trial Manager overseeing multiple trials or regions, responsible for strategic operational planning, vendor management, and program-level oversight. Primary objectives include shaping protocol and study design, leading vendor/CRO selection and negotiation, managing budgets and financial risk, mentoring junior staff, and ensuring audit readiness.



Responsibilities

Responsibilities extend to representing Clinical Operations externally and internally, proactively identifying and mitigating risks, and leading cross-functional initiatives.



Requirements

Requirements: S./B.A. in biological sciences with 8-10+ years industry experience, deep knowledge of FDA, EMA, ICH, GCP regulations, and proven experience managing global/multi-region trials and vendor relationships at a strategic level.



Preferred skills

Preferred skills include mentoring, influencing without authority, organizational excellence, and adaptability in a fast-paced environment.



High-value

High-value: Experience in clinical operations within biopharma, with a focus on small molecules, biologics, or targeted protein degradation therapies.



Location

Location: Onsite in Brisbane, CA, with 25% travel.

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