Nurix

Clinical Trial Manager (CTM)

Nurix • $157K — $168K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • B.S./B.A. in biological sciences with 5+ years of relevant industry experience
  • Ability to travel up to 25%
  • Knowledge of FDA, EMA, ICH, and GCP regulations
  • Experience managing clinical trials from start-up to close-out
  • Experience handling day-to-day CRO/vendor relationships
  • Strong analytical and problem-solving skills
  • Effective communicator with leadership abilities
  • Highly organized with multitasking capabilities
  • Ability to adapt in a small, fast-paced environment

Responsibilities

  • Take full ownership of assigned clinical trial(s) from protocol development to close-out
  • Manage daily relationships with CROs and vendors to ensure timelines and budgets are met
  • Build strong relationships with site investigators and study coordinators
  • Track and update stakeholders on trial progress
  • Address recruitment challenges proactively
  • Oversee study budget and vendor payments
  • Collaborate with Data Management on CRF content and deliverables
  • Draft and review study protocols and reports
  • Prepare for regulatory audits and inspections
  • Identify and mitigate project risks early

Benefits

  • Collaborative team culture
  • Hands-on approach encouraged
  • Focus on solutions and results
  • Supportive team environment
  • Flexibility in managing work responsibilities
Full Job Description
Clinical Trial Manager (CTM)

You'll take full ownership of your assigned trial(s) - from protocol development to close-out - with the autonomy to make daily calls and the support of an experienced team when it counts.

Position Description

This individual is responsible for the management of assigned clinical trial(s), leading the study team, vendors, clinical monitors, and clinical sites throughout the trial lifecycle.

The Opportunity
  • 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
  • Track trial progress and keep stakeholders updated on status
  • Monitor enrollment and address recruitment challenges as they arise
  • Manage study budget, forecasting, accruals, and vendor payments for your trial(s)
  • Partner with Data Management on CRF content, completion guidelines, and data deliverables
  • Draft and coordinate review of protocols, informed consents, CRFs, monitoring plans, and study reports
  • Prepare for and support regulatory agency audits and inspections
  • Flag risks early and recommend solutions before they become problems
  • Represent Clinical Operations at project team meetings

What You'll Bring
  • S./B.A. in biological sciences with 5+ years of relevant industry experience
  • Ability to travel as required for the program (25%)
  • Working knowledge of FDA, EMA, ICH, and GCP regulations and guidelines
  • Experience managing trials independently from start-up through close-out
  • Comfortable leading day-to-day CRO/vendor relationships
  • Strong analytical and problem-solving skills
  • Clear, confident communicator who can create direction for a study team
  • Ability to manage time demands, incomplete information, and shifting priorities
  • Highly organized, able to multi-task and prioritize independently
  • Thrives in a fast-paced, small-company environment

Salary Range: $157,700 - $168,200 annually

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.

Location: Onsite - Brisbane, CA

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

Nurix Therapeutics is a biotechnology company that is focused on the discovery, development, and commercialization of small molecule therapies that modulate the ubiquitin proteasome system (UPS) for the treatment of cancer and other diseases. The company's proprietary drug discovery platform is based on the use of DNA-encoded libraries (DELs) to identify small molecules that selectively bind to E3 ligases, which are key enzymes in the UPS. Nurix's lead drug candidate, NX-2127, is a first-in-class small molecule inhibitor of the CBL-B E3 ligase that is being developed for the treatment of solid tumors and hematological malignancies. The company was founded in 2013 and is headquartered in San Francisco, California.
Learn more about Nurix
Size
135 employees
Market Cap
$486 million
Industry
Net Income
-$43.2 million
Founded
2009
Revenue
$17.8 million
NASDAQ

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