Director, Late-Stage Program ManagementNew

Immunome-posted about 1 year ago

$200,000 - $231,000/Yr

Full-time • Senior

Bothell, WA

Professional, Scientific, and Technical Services

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The Director of Project Management for Late-Stage Programs at Immunome will play a crucial role in managing and advancing late-stage biotech programs through Phase 2 and Phase 3 clinical trials. This position requires a highly organized and experienced individual with a strong background in project management and late-stage drug development, collaborating closely with various teams to ensure the successful progression of pipeline candidates.

Lead the planning, execution, and monitoring of late-stage programs, from Phase 2 through Phase 3 clinical trials.
Develop comprehensive project plans, including timelines, milestones, and resource allocation.
Ensure programs are delivered on time, within scope, and within budget.
Coordinate cross-functional project teams, including clinical development, regulatory affairs, quality assurance, and external partners.
Facilitate regular team meetings to track progress, address issues, and ensure alignment with program goals.
Serve as the primary point of contact for internal and external stakeholders regarding program status and updates.
Identify potential risks and develop mitigation strategies to ensure program success.
Develop and manage program budgets, ensuring efficient use of resources.
Ensure all program documentation is complete, accurate, and compliant with regulatory requirements.
Support additional internal projects as the company grows, providing project management expertise.

PhD in Life Sciences (Biotechnology, Pharmacology, etc) recommended; other advanced degree (MBA, Master's) with relevant experience will also be considered.
Minimum of 10 years of experience in project management within the biotechnology or pharmaceutical industries, with a focus on late-stage programs.
Proven leadership experience with the ability to lead cross-functional teams and manage complex projects.
Strong interpersonal and communication skills, with the ability to influence and build relationships at all levels.
Excellent problem-solving and decision-making abilities.
Demonstrated ability to manage multiple priorities in a fast-paced environment.

High proficiency in project management tools and software (e.g., MS Project, Asana, Trello).
Extensive understanding of late-stage drug development processes and requirements.
Knowledge with regulatory requirements and industry standards (e.g., FDA, EMA).
Experience with data analysis and performance measurement techniques.
High proficiency in MS Office Suite (Word, Excel, PowerPoint).

Competitive salary range of $200,000 - $231,000 USD.
Equal opportunity employer with a commitment to diversity and inclusion.

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