Director of Project & Portfolio Management
Company: Outpace Bio
Location: Seattle
Posted on: January 24, 2025
Job Description:
About Outpace BioOutpace Bio is pioneering the future of cell
therapy for solid tumors by harnessing unrivaled AI-powered protein
design. Our mission is to program immune cells for enhanced
function inside patients, overcoming key barriers such as poor
tumor access, weak survival, antigen escape, and dose-related
toxicity. By creating and integrating modular, plug-and-play
technology assets, we are developing cell therapies with
unprecedented efficacy, transforming how engineered T cells
interact with cancer and the immune system to deliver life-changing
outcomes. Our multidisciplinary team of scientists, engineers,
coders, and cell therapy developers works at the cutting edge of
computational protein design, synthetic biology, and immunology.
Together, we are reimagining how cells function to unlock novel
therapeutic possibilities. Located in Seattle's vibrant biotech hub
overlooking scenic Lake Union, Outpace Bio is led by pioneers in
computational protein design and engineered cell therapies. Our
culture is built on a foundation of respect and inclusion, which
are fundamental to how we collaborate to revolutionize cell therapy
through groundbreaking innovation rooted in rigorous science.Our
Commitment to DiversityAt Outpace Bio, we believe that the highest
performing teams include people from a wide variety of backgrounds
and experiences. We are committed to cultivating an open, diverse,
and inclusive culture for all employees. Recognizing that the best
candidates do not always match all criteria of the job description,
we encourage you to apply if you think you would be a good fit for
the role and are inspired by our mission to cure disease by pushing
the boundaries of biology.Our MomentumIn August 2024, Outpace Bio
secured an oversubscribed $144 million Series B financing, led by
RA Capital Management and supported by a premier syndicate of life
science investors. This funding accelerates our pipeline of
programmed T cell therapies, including our lead candidate OPB-101,
a mesothelin-specific chimeric antigen receptor (CAR) T cell
enhanced by Outpace's proprietary OUTSMART, OUTLAST, OUTSPACER, and
OUTSAFE technologies. OPB-101 is advancing toward IND clearance and
first dosing in 2025 for patients with advanced platinum-resistant
ovarian cancers. The Series B investment also supports the
expansion of our pipeline, enabling us to develop additional
transformative therapies leveraging our innovative plug-and-play
technology platform.To enable this vision we are seeking a highly
motivated and experienced Director of Project & Portfolio
Management to help lead our cross-functional teams designing and
advancing programmed T cell therapies into the clinic. Reporting to
the Chief Business Officer, you will play a pivotal role in
managing drug development projects at both preclinical and clinical
stages. Partnering with Asset and Project Team Leaders, you will
foster a high-performing team environment while driving the
development and execution of integrated project plans across
functional disciplines. As the central source of project status,
you will ensure alignment, facilitate timely decision-making, and
escalate challenges as needed. In addition to managing individual
projects, you will contribute to building project management tools
and methodologies to support initiatives across our portfolio. This
role may also involve serving as an alliance manager for external
partners and vendors. We're looking for a detail-oriented problem
solver who thrives in dynamic environments and is passionate about
Outpace's mission to revolutionize cell therapy. If you're a
project or program management professional eager to work on
cutting-edge science with a collaborative team and grow your
career, this could be the role for you.Responsibilities (Position
responsibilities may include, but are not limited to):
- Project & Program Leadership: Partner with functional sub-team
leaders (CMC, Clinical, Research, Regulatory) to manage one or more
program sub-teams, ensuring alignment and successful execution of
development plans.
- Cross-Functional Planning & Integration: Collaborate with the
Program Leads or Asset Leaders to integrate functional sub-team
plans into a comprehensive cross-functional program plan. Identify
key milestones, interdependencies, critical paths, and risks, while
ensuring seamless execution.
- Risk & Timeline Management: Own program timelines across
cross-functional workstreams. Anticipate and mitigate risks, align
deliverables, and drive accountability for execution across project
teams. Utilize project management tools to facilitate
decision-making and communication.
- Stakeholder Communication & Reporting: Clearly communicate
program status, risks, and progress to key stakeholders, including
senior leadership and external partners. Establish a reporting
cadence to ensure visibility across the organization and prepare
materials for key meetings such as Portfolio Steering Committees
and Scientific Advisory Board reviews.
- Budget & Resource Management: Partner with finance to manage
program budgets, monitor spending, and guide resource allocation
decisions to meet project goals.
- Meeting Management & Documentation: Schedule and lead project
meetings. Maintain clear documentation of decisions, actions, and
progress through meeting minutes and action logs.
- Process Improvement: Help to build the project management
function by implementing tools, templates, and methodologies to
enhance team productivity and efficiency.
- Strategic Alliance & Vendor Management: Manage high-profile
partnerships and vendor relationships, including CDMOS, as needed.
Serve as the main point of contact for external stakeholders.
Ensure alignment on deliverables and successful execution.
- Portfolio Management: where possible contribute to program
strategy and life cycle management by helping to track the evolving
scientific landscape and treatment paradigms. Incorporate insights
from scientific, clinical, and investor presentations to inform
decision-making.Qualifications (Required):
- Bachelor's degree in a life science, engineering, technology,
business, or related field; an advanced degree (MS, PhD, or MBA) is
preferred.
- 10+ years of experience in the biotechnology or pharmaceutical
industry, with at least 5 years of direct project and portfolio
management in a science-based organization.
- Proven track record of leading complex, cross-functional
programs & projects through stage gates, ideally including
experience delivering against IND filings, early clinical, and the
cross-functional activities (Tech Ops, clinical, regulatory,
translational) to drive program expansion from Phase 1 to pivotal
development for cell therapies in oncology.
- Expertise in program and project management best practices,
including proficiency with tools such as Microsoft Project,
Smartsheet, or similar platforms.
- Strong analytical & problem-solving skills, with the ability to
synthesize complex information into actionable insights.
- Exceptional interpersonal skills, including the ability to
motivate teams, maintain positive working relationships with
collaborators, influence without authority, and effectively resolve
conflicts.
- Demonstrated ability to manage multiple projects, take
initiative, and work cross-functionally in a dynamic
environment.
- Excellent written and verbal communication skills, with the
ability to convey technical and strategic information (including
the core elements of engineered T cell therapies) effectively to
scientific and business audiences.
- Proven ability to identify risks proactively, prioritize tasks,
and drive issue resolution.
- Proven success in goal setting, prioritization, and time
management.
- Results-oriented, detail-oriented, and self-motivated, with the
ability to work independently with minimal supervision.
- Thrives in a fast-paced, dynamic environment, adapting
effectively to evolving priorities and ambitious
timelines.Qualifications (Preferred):
- PMP Certification preferred.
- Experience in nonclinical, CMC and clinical disciplines is
highly advantageous.
- Familiarity with FDA regulatory processes and clinical trial
management.
- Direct experience working on gene or cell therapy development
programs, with recent cell therapy experience being particularly
desirable.
- Prior experience in a direct management role is a plus.$200,000
- $240,000 a yearThe salary range is based on Outpace Bio's
reasonable estimate of base salary for this role at the time of
posting. Actual base salary will be based on a variety of factors
including skills, experience, and other related factors permitted
by law.Working at Outpace offers an exciting opportunity to
contribute to groundbreaking research that has the potential to
transform the lives of people around the world.Outpace Bio Total
RewardsFull time employees and their eligible dependents may enroll
in Outpace's medical, dental, vision, life insurance, disability,
flexible spending account, and 401k plan. In addition, employees
may receive stock option grants to be outlined in their offer of
employment. Outpace employees enjoy flexible PTO, paid sick leave
which complies with local requirements, and fifteen paid holidays
plus a winter shutdown. Outpace also offers a generous paid
parental leave policy to all regular full-time employees.Outpace
Bio is committed to a diverse workforce. Employment decisions
regarding recruitment and selection will be made without
discrimination based on race, color, religion, national origin,
gender, age, sexual orientation, physical or mental disability,
genetic information or characteristic, gender identity and
expression, veteran status, or other non-job related
characteristics or other prohibited grounds specified in applicable
federal, state and local laws.Applicants must be authorized to work
in the United States. If you are legally authorized to work in the
United States now, or in the future without any form of
sponsorship, we encourage you to apply.
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Keywords: Outpace Bio, Edmonds , Director of Project & Portfolio Management, Executive , Seattle, Washington
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