Senior Director, Program Management Lead - Commercial
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Taysha Gene Therapies
Chicago, IL, US
Summary
The Senior Director will lead integrated program management across the Commercial organization to ensure alignment on priorities, milestones, and launch readiness. They will partner with functional leaders to drive execution, manage risks, and facilitate governance across the enterprise.
Job Description
Overview of Position
The Senior Director, Program Management Lead for Commercial is responsible for leading integrated program management across the Commercial organization and ensuring Commercial priorities, milestones, dependencies, risks, and decisions are effectively coordinated with the broader enterprise program.
This role will partner closely with Commercial leadership and functional leads across Commercial, Market Access, Patient Services, Marketing, and other relevant functions, as well as key cross-functional partners such as Medical Affairs and the PMO. The Commercial Program Management Lead will own the integrated Commercial program and workstream plan and drive the planning, coordination, governance, and execution required to support commercialization and launch readiness.
The role will also oversee program management of launch-readiness activities, including management of external launch-readiness support as applicable, while Commercial and functional leaders retain accountability for commercial strategy, functional decisions, and deliverables.
As a senior member of the PMO organization, this individual will report to the Head of PMO and serve as the primary PMO partner to the Commercial organization.
Essential Duties
- Own the integrated Commercial program and workstream plan, including key milestones, timelines, dependencies, risks, decisions, and critical-path activities across Commercial functions.
- Lead integrated Commercial program management, connecting activities across Marketing, Market Access, Patient Services, Commercial Operations, and other relevant Commercial functions and cross-functional partners.
- Drive launch-readiness program management and execution, ensuring readiness activities, decision points, dependencies, risks, and deliverables are integrated and actively managed across the organization.
- Oversee external launch-readiness program management support and vendors, as applicable, to ensure alignment with company priorities, readiness criteria, timelines, and governance.
- Integrate Commercial milestones and dependencies with the enterprise Integrated Program Plan, partnering with the Head of PMO and other Program Management Leads to maintain alignment across the broader program.
- Establish and facilitate Commercial program governance, including leadership and cross-functional forums required to drive decisions, resolve issues, monitor readiness, and maintain execution against priorities.
- Identify, manage, and escalate key program risks, dependencies, resource constraints, and decisions requiring Commercial or executive leadership attention.
- Partner with Commercial leadership and functional leaders to translate strategic priorities and decisions into clear, executable plans while maintaining appropriate functional accountability.
- Drive cross-functional coordination with key partner functions outside Commercial, including Medical Affairs and others, to ensure Commercial requirements and dependencies are identified and incorporated into program planning.
- Provide clear and concise program reporting to senior leadership, including progress against critical milestones, launch readiness, emerging risks, decisions required, and areas requiring escalation.
- Lead and/or oversee Commercial project management resources or other relevant vendors, as the organization evolves, ensuring consistent program management standards, tools, and ways of working.
- Partner with the broader PMO organization to strengthen program governance, planning processes, tools, reporting, and execution discipline across Taysha.
Skill & Education Requirements
- Bachelor’s degree required; advanced degree such as an MBA, M.S., or other relevant graduate degree preferred.
- 10+ years of experience in the pharmaceutical, biotechnology, or life sciences industry, with level commensurate with Senior Director or Executive Director responsibilities.
- Significant experience in program/project management, commercialization, launch readiness, commercial operations, or a closely related cross-functional leadership role within the biopharmaceutical industry.
- Demonstrated experience supporting late-stage development through commercialization and product launch, preferably within specialty, rare disease, advanced therapy, or similar complex therapeutic areas.
- Strong understanding of the activities and interdependencies required for commercialization, including Marketing, Market Access, Patient Services, Commercial Operations, Medical Affairs, and related functions.
- Demonstrated ability to lead complex, cross-functional programs in which functional leaders retain decision-making and deliverable accountability.
- Experience developing and managing integrated program plans, including critical paths, milestones, dependencies, risks, decisions, and launch-readiness criteria.
- Strong executive presence and demonstrated ability to work effectively with senior and executive leadership, facilitate decision-making, and appropriately escalate issues.
- Demonstrated success operating in a fast-paced, dynamic, and evolving organization, with the ability to create structure, establish priorities, and drive execution through ambiguity.
- Exceptional communication, facilitation, organizational, and stakeholder-management skills.
- Ability to influence effectively across organizational boundaries and build strong partnerships across functional teams without relying on direct authority.
- Experience managing project/program management personnel and/or external program management or commercialization vendors preferred.
- PMP or other relevant program management certification preferred but not required.
This role can be performed remotely or based from Chicago IL. Expected travel 25%
Base compensation range at time of posting: $255,000 – 285,000 annual salary, depending on experience and qualifications.
The actual base salary depends, in part, on the successful candidate’s qualifications for the role, including education and experience. Taysha offers a comprehensive compensation and benefits program to eligible employees, including Individual Stock Option awards; ESPP program; eligibility to participate in performance bonus program; Taysha-sponsored 401(k) with matching contribution; eligibility for medical, dental, vision and prescription drug benefits and a generous vacation/holiday schedule.
Note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
Taysha is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Taysha are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate.
Taysha Gene Therapies is a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system. Its lead clinical program TSHA-102 is in development for Rett syndrome, a rare neurodevelopmental disorder with no approved disease-modifying therapies that address the genetic root cause of the disease. With a singular focus on developing transformative medicines, Taysha aims to address severe unmet medical needs and dramatically improve the lives of patients and their caregivers. The Company’s management team has proven experience in gene therapy development and commercialization. Taysha leverages this experience, its manufacturing process and a clinically and commercially proven AAV9 capsid in an effort to rapidly translate treatments from bench to bedside.
Founded
2020
Company size
51-200 employees
Industry
Biotechnology
Org type
Public Company
Headquarters
Dallas, TX
Taysha Gene Therapies is a clinical-stage biotechnology company focused on advancing adeno-associated virus (AAV)-based gene therapies for severe monogenic diseases of the central nervous system. Its lead clinical program TSHA-102 is in development for Rett syndrome, a rare neurodevelopmental disorder with no approved disease-modifying therapies that address the genetic root cause of the disease. With a singular focus on developing transformative medicines, Taysha aims to address severe unmet medical needs and dramatically improve the lives of patients and their caregivers. The Company’s management team has proven experience in gene therapy development and commercialization. Taysha leverages this experience, its manufacturing process and a clinically and commercially proven AAV9 capsid in an effort to rapidly translate treatments from bench to bedside.
Founded
2020
Company size
51-200 employees
Industry
Biotechnology
Org type
Public Company
Headquarters
Dallas, TX