Consultant, Project Management

ABOUT THE COMPANY

Winnow Therapeutics is a VC-backed, next-generation immunotherapy company focused on transforming the treatment of autoimmune diseases. Founded by world-renowned scientific leaders and supported by top-tier investors, we are advancing a new class of medicines aimed at restoring immune balance and redefining outcomes for patients with autoimmune conditions. By combining proven science with innovative approaches, we aim to deliver deep and lasting responses. We are building our founding team in Boston, Massachusetts, offering a unique opportunity to join at an early stage to help shape the future of the company.

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ABOUT THE ROLE

Winnow Therapeutics is seeking an experienced project management consultant for a short-term assignment focused on developing an integrated project plan with a focus on IND-enabling activities. The consultant will work with functional leads to translate development plans into detailed, actionable workplans. The primary focus will be schedule development, cross-functional integration, dependency mapping, critical-path analysis, and risk identification.

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RESPONSIBILITIES

• Develop detailed project plans in collaboration with functional leads and program management
• Integrate plans across nonclinical, CMC, regulatory, and other relevant workstreams into a coordinated master timeline
• Identify key milestones, dependencies, decision points, long-lead activities, and potential schedule risks
• Facilitate planning discussions with internal teams and external partners to validate timelines, assumptions, deliverables, and resource requirements
• Identify planning gaps, sequencing conflicts, and unresolved dependencies, and work with functional owners to establish mitigation actions
• Develop practical project-management tools, including milestone trackers, risk and decision logs, and responsibility matrices
• Provide a clear handoff of the integrated plan and supporting materials to Winnow’s existing program management team

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QUALIFICATIONS

• BA/MA/PhD in a related field with 7+ years of project management experience supporting IND-enabling development
• Demonstrated track record in achieving IND submission within the developed program timelines
• Familiarity with FDA/EMA frameworks, GxP requirements (GLP, GMP, GCP), and how regulatory milestones gate downstream work
• Demonstrated ability to develop complex timelines, and manage cross-functional stakeholders in a fast-paced biotech environment
• Exceptional organizational skills with proficiency in project management tools (e.g., Smartsheet, Monday.com, or similar)
• Experience in autoimmune, immunology, or other biologics-focused therapeutic areas preferred

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SKILLS & COMPETENCIES

• Impactful skills and demonstrated ability to help build key company capabilities supporting leadership and scientists with data gathering, analysis, and interpretation
• Excellent analytical, problem solving and critical thinking skills, including an ability to combine attention to detail with a big picture perspective
• Ability to thrive in a fast-paced, innovative, and evolving environment while remaining flexible, proactive, and resourceful
• Adept at prioritizing and managing multiple tasks simultaneously, integrating cross-functional collaboration and balancing competing priorities effectively
• Collaborative and team-oriented mindset with a desire to positively impact a new company’s evolving culture​

How to Apply

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