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Associate Director​/Director, Clinical Project Delivery

Job in North Bothell Area, Snohomish County, Washington, 98021, USA
Listing for: Immunome, Inc.
Full Time position
Listed on 2026-10-05
Job specializations:
  • Healthcare
    Healthcare Management
  • Management
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 186000 - 212000 USD Yearly USD 186000.00 212000.00 YEAR
Job Description & How to Apply Below
Associate Director / Director, Clinical Project Delivery

Bothell, Washington, United States

Company Overview

Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA;

IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.

Position Overview

The Associate Director / Director, Clinical Project Delivery provides hands-on operational leadership for the execution of one or more of Immunome's clinical trials, facilitating all aspects of cross-functional clinical trial delivery from planning and initiation through completion - ensuring studies are executed on time, within budget, and in compliance with regulatory requirements and corporate objectives.

This role acts as the primary point of accountability for study-level timelines, enrollment projections, budgets, and vendor performance for assigned trials, serving as a subject matter expert in clinical trial delivery and vendor oversight.

The Associate Director / Director may be assigned to lead or support one or more development programs as well as functional or departmental initiatives.

Responsibilities Clinical Project Delivery
  • Own cross-functional facilitation of clinical study teams through the trial lifecycle.
  • Own study-level timeline development, tracking, and reporting for assigned trials.
  • Develop and maintain enrollment graphs and dashboards, ensuring accuracy and timely updates to inform decision-making.
  • Monitor project delivery metrics (timelines, milestones, enrollment, budget adherence, TMF and vendor KPIs) and drive corrective action when studies are at risk.
  • Lead cross-functional planning, execution, and delivery of assigned clinical trials on time, within budget, and to quality standards .
  • Identify operational risks and implement mitigation strategies to ensure successful trial delivery.
Clinical Operations Leadership
  • Support resource planning and capability building to meet the demands of a rapidly expanding clinical portfolio.
  • Champion a culture of accountability, collaboration, and continuous improvement.
  • May be assigned one or more direct reports with the expectation of providing coaching, mentorship, and development.
  • Guide and mentor new and junior Clinical Operations team members.
  • Own CROs and central lab vendor relationships and oversight for assigned studies.
  • Owns vendor identification, selection, contracting, and onboarding activities in partnership with Finance, Legal, and clinical study teams.
  • Manage and monitor vendor performance against contractual obligations, operational timelines, and quality and performance metrics.
  • Lead governance meetings, oversight activities, and drive issue escalation and resolution to ensure timely and effective trial execution.
Quality Assurance and Regulatory Compliance
  • Ensure adherence to ICH-GCP, FDA, EMA, and global regulatory requirements for assigned trials.
  • Partner with Quality Assurance and the Clinical Study Team to ensure ongoing inspection-readiness and implement corrective actions as needed.
  • Drive operational excellence to ensure data integrity and consistent trial conduct across assigned trials.
Cross-Functional Collaboration
  • Align cross-functionally on program objectives and study execution plans.
  • Partner with Clinical Site & Trial Operations, Clinical Field Monitoring & Trial Operations, and Clinical Development Systems to align on trial delivery strategy and execution.
  • Partner with cross-functional teams to identify and mitigate study delivery risks.
  • Provide study-level operational input into program-level discussions and decisions.
  • Support regulatory submissions (INDs, NDAs, BLAs) and health authority interactions as needed for assigned studies.
Budget and Resource Management
  • Partner with Finance to manage and forecast study-level budgets, including change orders ensuring alignment with corporate priorities and program timelines.
  • Maintain financial oversight for vendor and study-related activities, strictly tracking,…
Position Requirements
10+ Years work experience
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