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 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.