Director, Program Management

Immunomeinc; Bothell (WA); On-site; USD 215,000 - 242,000; Full time

Job summary

Immunome, Inc. in Washington State seeks a Director of Program Management to drive cross-functional planning across ADC and radiopharmaceutical assets, overseeing integrated development plans, CMC timelines, and regulatory strategies.

The role requires 8–10 years in biotech/pharma program management, experience with both early and late-stage development, and strong cross-functional leadership. Strong communication and vendor management are essential.

Qualifications

• Bachelor’s degree required in a technical or scientific field; advanced degree preferred.
• 8–10 years of project and program management experience in biotech/pharma.
• Formal project management training or certification (e.g., PMP) desirable.

Responsibilities

• Serve as the program manager for ADC asset, owning the integrated development plan across clinical, nonclinical, CMC, and regulatory workstreams.
• Drive transition from early to late-stage development with governance cadence to meet late-stage requirements.
• Build and maintain integrated program timeline and critical path; identify sequencing conflicts and long-lead items.
• Coordinate cross-functional teams and drive stage-gate readiness and risk mitigation.

Skills

Cross-functional leadership

Program management

CMC project management

Drug development knowledge

Regulatory submissions

PM tools (Smartsheet/MS Project/Asana)

Education

Bachelor’s degree in a technical or scientific field

Advanced degree (PhD, MS, PharmD, MBA) preferred

Tools

Smartsheet

MS Project

Asana

Job description

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 Director, ProgramManagementis a hands-on program manager responsible for driving cross-functional planning and execution across two assets atdifferent stagesof development. First, this role will serve as the program manager for our first ADC program as it transitions from early to late-stage development, building the integrated development plan, operating cadence, and governance infrastructurerequiredto carry the asset forward. Second, this role will support an early-stage asset within our radiopharmaceutical portfolio, serving as both the program manager and the CMC project manager from candidateselectionthrough IND-enabling activities and early clinical evaluation.

Responsibilities

ADC Program Management – Early to Late-Stage Transition

• Serve as the program manager for our first ADC asset, owning the integrated development plan across clinical, nonclinical, CMC, and regulatory workstreams.
• Drive the operational transition from early to late-stage development, evolving team structure, planning rigor, and governance cadence to meet late-stage requirements.
• Build and maintain the integrated program timeline and critical path; proactively identify sequencing conflicts, resourcing constraints, and long-lead items.
• Drive preparation for key stage-gates, health authority interactions, and governance decision points, ensuring materials and recommendations are decision-ready.

Radiopharmaceutical Program Management – Early Stage

• Serve as the program manager for an early-stage radiopharmaceutical asset, supporting the cross-functional team from candidate selection through IND-enabling activities and early clinical evaluation.
• Develop the integrated early development plan spanning discovery deliverables, nonclinical studies, CMC, regulatory strategy, and first-in-human readiness.
• Coordinate workstreams into a single critical path and drive candidate selection and IND stage-gate readiness.
• Anticipate and plan for the operational and supply considerations specific to radiopharmaceutical development.

CMC Project Management

• Represent CMC on the core product development team, serving as the point of accountability for CMC deliverables, timelines, and risks.
• Develop and drive integrated CMC timelines to meet the needs of the product development team, coordinating activities across CMC functions.
• Serve as the primary liaison to contract manufacturing organizations and other external partners, managing scope, deliverables, and schedule adherence.
• Direct the CMC budgeting process for the program and manage project spend to target.

Cross-Functional Team Coordination

• Coordinate cross-functional teams spanning research, nonclinical, CMC, clinical development, clinical operations, regulatory affairs, quality assurance, and external partners.
• Facilitate core team and sub-team meetings; drive agendas, capture decisions and actions, and hold the team accountable to commitments.
• Foster a collaborative, transparent, and high-accountability team environment across both programs.

Stakeholder Engagement and Reporting

• Serve as the primary point of contact for internal and external stakeholders on program status, ensuring transparent communication of progress, risks, and mitigation plans.
• Prepare and present program updates, performance metrics, and outcomes to senior leadership and portfolio review forums.
• Direct the preparation of program dashboards, timelines, and executive presentations.

Risk and Issue Management

• Proactively identify program risks across technical, operational, supply, and regulatory dimensions.
• Develop, own, and drive mitigation and contingency strategies throughout the program lifecycle.
• Maintain and actively manage the program risk register; elevate with clear options and recommendations.

Budget and Resource Management

• Partner with Finance and functional leaders to develop and manage program budgets and forecasts; track spend versus plan and support prioritization decisions.
• Support program resourcing and capacity planning across functions; flag constraints early and propose options to protect the critical path.
• Secure and allocate resources to ensure efficient use across both programs.

Documentation and Compliance

• Ensure all program documentation is complete, accurate, and compliant with regulatory requirements.
• Maintain detailed records of program activities, including progress reports, meeting minutes, program decisions, and action items.
• Ensure programs adhere to industry standards, GxP expectations, and regulatory guidelines.

Program Management Operating Model

• Develop and implement metrics to evaluate program performance and use data-driven insights to recommend strategic adjustments.
• Contribute to the development and adoption of program management best practices, templates, dashboards, and tools across the portfolio.
• Support additional projects and initiatives within the project management organization as the company continues to grow.

Qualifications

• Bachelor’s degree required in a technical or scientific field such as chemistry, chemical engineering, pharmaceutical sciences, biology, or a related life sciences discipline; advanced degree (PhD, MS, PharmD, MBA) preferred.
• Formal project management training or certification (e.g., PMP) highly desirable.
• 8 to 10 years of project and program management experience within the biotechnology or pharmaceutical industry preferred, including both drug development program management and CMC project management experience.

Knowledge and Skills

• Demonstrated success managing programs across multiple stages of development, including experience supporting the transition from early to late-stage.
• Direct, hands-on CMC project management experience, including ownership of manufacturing timelines and external manufacturing partnerships.
• Proven track record driving cross-functional core teams and managing complex, interdependent programs in a matrixed environment.
• Strong working knowledge of drug development functions and their key interdependencies, along with familiarity with FDA and EMA requirements and industry standards.
• Excellent cross-functional communication skills, with the ability to influence and build relationships at all levels of the organization.
• Demonstrated ability to manage multiple priorities in a fast-paced environment, with strong problem-solving and decision-making abilities.
• Proficiency in project management tools and software (e.g., Smartsheet, MS Project, Asana) and high proficiency in MS Office Suite (Word, Excel, PowerPoint).

Preferred Experience

• Experience with antibody drug conjugates, radiopharmaceuticals, or other targeted oncology modalities.
• Oncology development experience and exposure to both large molecule and small molecule programs.
• Experience supporting regulatory submissions and health authority interactions (e.g., IND, CTA, briefing packages).
• Experience in a small to mid-size biotech environment where building process and infrastructure is part of the role.

Washington State Pay Range

$214,962 — $242,116 USD

E/E/O

Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

E-Verify

Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).