Associate Director/Director, Clinical Project Delivery
Listed on 2026-10-05
-
Healthcare
Healthcare Management -
Management
Healthcare Management
Bothell, Washington, United States
Company OverviewImmunome 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.
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.
- 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.
- 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.
- 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.
- 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,…
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).