Director of Program Management

Quetzal Therapeutics; United States; Remote; USD 140,000 - 230,000; Full time

Benefits offered by this job

Comprehensive medical, dental, and视on

Health and flexible spending account

Paid time off, sick leave, holidays

Voluntary benefit options

Job summary

Quetzal Therapeutics is seeking a Director of Program Management to lead integrated development plans, coordinate cross-functional teams, and manage timelines across NDA filings and launch activities. The role requires deep drug development knowledge and proven leadership in a fast-paced biotech environment.

You will partner with Clinical Operations, Regulatory, CMC, and QA to drive risk mitigation, executive communications, and on-time delivery of critical program milestones.

Qualifications

• Bachelor's degree in Life Sciences, Public Health, Pharmacy, Engineering, or related discipline.
• 8+ years of experience in biotechnology, pharmaceutical, or life sciences environments.
• 5+ years of program or project management experience supporting drug development programs.
• Demonstrated understanding of clinical development and regulatory processes.
• Strong leadership, communication, and organizational skills.

Responsibilities

• Develop and maintain integrated development plans for Quetzal's development programs.
• Define program strategy with cross-functional teams and translate into executable plans.
• Identify program risks, dependencies, and mitigation strategies; maintain risk logs.
• Drive cross-functional execution to meet milestones and timelines.
• Support portfolio planning, budgeting, and resource allocation.
• Develop program dashboards and executive-facing reports; communicate status to leadership.
• Coordinate governance meetings and ensure timely reporting and decisions.

Skills

Leadership

Cross-functional collaboration

Communication

Drug development knowledge

Regulatory awareness

Education

Bachelor's degree in Life Sciences or related field

Tools

PMP certification

MS Project/Clarity

Job description

Quetzal Therapeutics is a biopharmaceutical company focused on the development of treatment for rare diseases including hematologic malignancies. The company’s lead product is QTX-2101, a novel paradigm for treating patients with Acute Promyelocytic Leukemia (APL) for which the company initiated a Phase III clinical trial in December 2025.. Quetzal is also developing a pre-clinical asset QTX-2102, an advanced, next-generation antifungal and antiparasitic therapy designed to enhance efficacy while minimizing toxicity. Our mission is to push the boundaries of treatment possibilities, delivering hope and life-changing solutions to those who need them most.

About the role

Reporting to the Vice President, Global Program Leadership, the Director will partner with functional leaders across Clinical Development, Regulatory Affairs, CMC, Clinical Operations, Medical Affairs, Quality, Biometrics, and external vendors to ensure the successful planning and execution of Quetzal's development strategy.

This role will be responsible for maintaining integrated program plans and detailed project plans (i.e. NDA filing, commercial launch planning),driving cross-functional alignment, managing risks and dependencies, and delivering clear communications to executive leadership. The ideal candidate combines strong drug development knowledge with exceptional project leadership capabilities and thrives in a fast-paced biotechnology environment.

Why Join Us

This is an opportunity to play a visible, hands-on role in shaping our Clinical Operations team and strengthening our company’s processes. You will partner with leadership and help build a team grounded in compliance, collaboration, and continuous improvement.

What you'll do

Program Management & Execution

• Partner with the VP, Global Program Leadership to develop and maintain integrated development plans for Quetzal's development programs.
• Partner with thecross-functionalProgramTeam functional leadersto define program strategy, conduct scenario planning, and translate strategy into executable plans to achieve program objectives
• Identify and manage program-level risks, assumptions, and interdependencies; support cross-functional mitigation planning, issue resolution, and formal Risk Log generation/maintenance
• Drive cross-functional execution against approved program objectives, milestones, and timelines.
• Support portfolio planning and strategic program initiatives.
• Ensure alignment across Clinical Development, Regulatory Affairs, CMC, Quality, and other key functions.
• Proactively identify and communicate risk and decision-points with mitigation opportunities and impact assessment
• Develop and manage integrated program timelines and critical path analyses.
• Identify interdependence across functional workstreams.
• Build scenario analyses and contingency plans to support decision-making.
• Track program progresses and proactively identifies risks, delays, and resource challenges.

Cross-Functional Team Management

• Coordinate and facilitate cross-functional program team meetings.
• Drive accountability and follow-up on key decisions and action items.
• Promote collaboration among internal stakeholders and external partners.
• Ensure timely communication of goals, deliverables, and program updates.
• Support vendor oversight, providing PM-to-PM partnership for timely and cost effective delivery of program needs

Key functional project plans and sub-team facilitation:

• Support Program Team and individual functions in critical project plan generation, ensuring alignment with overall development plan.
• Regulatory Submission Plan:
• Together with Regulatory, generate and oversee NDA submission plan and ex-US submission plans, identify critical path activities and potential risk, support scenario planning
• Ensure timely cross-functional delivery against submission plan
• Support Regulatory in vendor oversight
• Prepare dashboards and graphics for Program Team and executive communication and discussions
• Commercial Launch Plan:
• Together with key functional stakeholders, support generation and oversight of commercial launch plan
• Aligning with launch plan with submission plan and integrated program plan and ensuring timely launch-readiness and proactively identifying impact of shifts across plans
• Identify key gaps and risks to plan with proactive escalation and mitigation

Governance & Executive Reporting

• Develop program dashboards, status reports, and support generation of executive presentations.
• Support governance meetings and portfolio reviews.
• Support budgeting, forecasting, and resource planning activities.
• Monitor program expenditures and key vendor engagements.
• Collaborate with Finance and functional leaders on resource allocation and planning.
• Support evaluation of outsourcing strategies and vendor performance.
• Drive implementation of program management best practices, tools, and processes.
• Promote operational excellence across development teams.
• Contribute to building Quetzal's program management capabilities as the organization grows.

Qualifications

Required

• Bachelor's degree in Life Sciences, Public Health, Pharmacy, Engineering, or related discipline.
• 8+ years of experience in biotechnology, pharmaceutical, or life sciences environments.
• 5+ years of program or project management experience supporting drug development programs.
• Demonstrated understanding of clinical development and regulatory processes.
• Strong leadership, communication, and organizational skills.
• Proven ability to influence cross-functional teams without direct authority.

Preferred

• Oncology, hematology, or rare disease experience.
• Phase II or Phase III development experience.
• PMP certification.
• Advanced degree (MS, MPH, MBA, PharmD, or PhD).
• Startup or emerging biotechnology company experience , governance.
• Experience in startup or high-growth company environments.

Benefits & What We Offer

Quetzal Therapeutics offers eligible employees a competitive benefits package designed to support their health, wellbeing, and work-life balance. Our benefits include:

• Comprehensive medical, dental, and vision coverage
• Health and flexible spending account options
• Paid time off, sick leave, and company holidays
• Additional voluntary benefit options

Benefits and eligibility may vary based on employment status, location, and applicable plan terms and company policies.

Equal Opportunity Employer

Quetzal Therapeutics is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, or other characteristics protected by federal, state, or local law.