Senior Project Manager - PMO (Phoenix)

Caris Life Sciences•Tempe, AZ

1d•Onsite

About The Position

The Senior Project Manager is a strategic leader responsible for driving enterprise-level initiatives that advance Caris’ precision medicine portfolio and operational capabilities. This role leads programs from concept through execution, aligning business goals, product requirements, regulatory and quality expectations, technical deliverables, and launch readiness across internal and external stakeholders. The ideal candidate brings strong program leadership, sound judgment in regulated and fast-moving environments, and the ability to translate ambiguity into clear plans, decisions, accountability, and results. This individual will partner closely with leaders across product development, translational science, bioinformatics/software, laboratory operations, quality, regulatory, and commercial-facing functions to deliver programs that are high quality, on time, and aligned to business and patient impact.

Requirements

Bachelor’s degree in healthcare, life sciences, business, information systems, or a related field, or equivalent combination of education and experience.
8+ years of direct experience in a project/program management, product management, SaaS, implementation, or related roles, including significant experience leading complex cross-functional initiatives within healthcare industry.
Proven ability to influence cross-functional stakeholders, drive alignment, and deliver results in environments with competing priorities and ambiguity.
Proficiency in Microsoft Office Suite including Project, Word, Excel, Outlook, and PowerPoint.
Ability to travel up to 20%.

Nice To Haves

Formal project management training or PMP certification.
Prior experience in Agile or hybrid methodologies Lean Six Sigma, or similar, training or certification.
Experience documenting processes.
Familiarity with health information systems and related platforms, such as EHR, LIMS, LIS, or other laboratory/clinical systems.
Working knowledge of applicable regulatory and quality frameworks (e.g., CLIA, CAP, GMP, GCP, IVDR, HIPAA), related design control/validation expectations, and how they impact day-to-day operations and deliverables.

Responsibilities

Lead complex, regulated programs from initiation through execution, ensuring alignment on scope, milestones, risks, dependencies, resource needs, and business outcomes.
Translate strategic objectives and product requirements into actionable project plans, governance structures, timelines, and workstream deliverables.
Partner with leaders across product development, translational science, laboratory operations, bioinformatics/software, quality, regulatory, and other business functions to drive execution in a highly collaborative environment.
Drive program governance by facilitating core team meetings, documenting key decisions and actions, maintaining accountability, and escalating critical issues with recommended solutions.
Manage interdependencies across teams and vendors, proactively identifying execution risks, resource gaps, and competing priorities that may impact delivery.
Develop and maintain project artifacts including integrated plans, milestone trackers, decision logs, status reports, and executive-ready updates.
Monitor program health and performance, communicate progress to stakeholders at all levels, and lead structured health checks to keep initiatives on track.
Support product development and launch readiness efforts by aligning cross-functional deliverables, operational handoffs, and implementation planning.
Drive continuous improvement in project delivery practices, team coordination, communication cadence, and launch execution.
Build strong working relationships across the organization through credibility, responsiveness, sound judgment, and a solutions-oriented approach.