Director of Early-Stage Program Management

2 weeks ago

Bothell, Washington, United States Immunome Inc Full time

Immunome Inc is a clinical-stage targeted oncology company dedicated to developing innovative therapies for cancer patients.

We are advancing a portfolio of therapeutics, leveraging leadership experience in the design, development, and commercialization of targeted cancer therapies.

The Associate Director of Early Programs, Project Management will play a critical role in guiding early-stage biotech programs from candidate selection through Phase 1 trials.

This position requires a dynamic and detail-oriented individual with a robust background in project management and early-stage drug development.

The successful candidate will work closely with research teams, cross-functional departments, and external partners to ensure the successful advancement of pipeline candidates.

This position reports to the Senior Vice President of Project and Program Management and supports additional projects within the broader project management and research teams, contributing to the strategic objectives of the company.


Key Responsibilities:
  • Oversee the planning, execution, and monitoring of early-stage programs, from candidate selection through Phase 1 trials.
  • Develop comprehensive project plans, including timelines, milestones, and resource allocation.
  • Coordinate cross-functional project teams, including research scientists, clinical development, regulatory affairs, and external partners.
  • Communicate program progress, challenges, and solutions to senior leadership and other stakeholders.
  • Manage stakeholder expectations and resolve conflicts that may arise during program execution.

Requirements:
  • Minimum of 7 years of experience in project management within the biotech or pharmaceutical industries, with a focus on early-stage programs.
  • Proven leadership experience with the ability to lead cross-functional teams and manage complex projects.
  • Demonstrated ability to manage multiple priorities in a fast-paced environment.
  • Proficiency in project management tools and software (e.g., MS Project, Asana, Trello).
  • Familiarity with regulatory requirements and industry standards (e.g., Regulatory submission experience preferred).
  • Experience with data analysis and performance measurement techniques.
  • High proficiency in MS Office Suite (Word, Excel, PowerPoint).

Preferred Qualifications:
  • Advanced Degree in Life Sciences, Biotechnology, Pharmacology, or a related field.

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