Manager, Clinical Project Delivery

About the role

The Manager, Clinical Project Delivery provides hands-on operational support for the execution of one or more of Immunome’s clinical trials, supporting cross-functional clinical trial delivery from planning and initiation through completion—to help ensure studies are executed on time, within budget, and in compliance with regulatory requirements and corporate objectives. This role contributes to study-level timeline management, helps maintain enrollment projections, supports budget management and vendor performance oversight for assigned trials. The Manager, Clinical Project Delivery may support one or more studies under the guidance of an Associate Director or above.

Responsibilities

• Clinical Project Delivery Support cross-functional facilitation of clinical study teams through the trial lifecycle.
• Assist with study-level timeline development, tracking, and reporting for assigned trials.
• Help develop and maintain enrollment graphs and dashboards, ensuring accuracy and timely updates to inform decision-making.
• Help monitor project delivery metrics (timelines, milestones, enrollment, budget adherence, vendor KPIs) and drive corrective action when studies are at risk.
• Support cross-functional planning, execution, and delivery of assigned clinical trials on time, within budget, and to quality standards.
• Help identify operational risks and implement mitigation strategies to ensure successful trial delivery.
• Champion a culture of accountability, collaboration, and continuous improvement.
• Vendor Management Support CRO and Central lab vendor relationships and oversight for assigned studies.
• Assist with vendor identification, selection, contracting, and onboarding activities in support of Finance, Legal, and clinical study teams.
• Help monitor vendor performance against contractual obligations, operational timelines, and quality and performance metrics.
• May support governance meetings, oversight activities, issue escalation, and resolution to ensure timely and effective trial execution.
• Quality Assurance and Regulatory Compliance Help ensure adherence to ICH-GCP, FDA, EMA, and global regulatory requirements for assigned trials.
• May work with Quality Assurance and the Clinical Study Team to ensure ongoing inspection-readiness and implement corrective actions as needed.
• Support data integrity and consistent trial conduct across assigned trials.
• Cross-Functional Collaboration Participate in cross-functional alignment of program objectives and study execution plans.
• Support cross-functional teams to help identify and mitigate study delivery risks.
• Budget and Resource Management Work with CPD and Finance to support management and forecasting of study-level budgets, including change orders, ensuring alignment with corporate priorities and program timelines as assigned.
• Assist with financial oversight for vendor and study-related activities.
• Help track and report on budget adherence for assigned studies.

Qualifications