Senior Director, Research Strategy and Operations (Core Team Leader – Liquid Biopsy)

Tempus AI•Boston, MA

21d•$192,000 - $264,000

About The Position

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. We are seeking an industry veteran to serve as the Core Team Leader (CTL) for our Liquid Biopsy (xF) portfolio. In this high-impact role, you will act as the “Leader of the Product Development Lifecycle." You will move beyond simple project coordination to assume full accountability for the execution and commercial launch of complex regulated diagnostic products. You will lead a cross-functional Core Team - comprising leaders from R&D, Clinical, Regulatory, Quality, Software, and Operations - to navigate the journey from concept to commercialization. This is a matrix leadership role. You will partner with a Product Manager (who defines market strategy) and a Project Manager (who manages tactical schedules), while you provide the strategic glue, operational oversight, and decision-making authority required to deliver the product to market.

Requirements

Advanced degree (PhD, MD, MS) in Genetics, Molecular Biology, or Engineering required.
10+ years in the life sciences/diagnostics industry, with at least 4+ years serving as a Core Team Leader, Product Development Lead, or Program Director in a matrixed environment.
Deep experience in Oncology Diagnostics, NGS, or Liquid Biopsy is essential.
Experience navigating FDA Class II/III medical device development (PMA/510k) is highly preferred.
Expert knowledge of Phased-Gate/Stage-Gate development cycles. You understand the difference between tracking a timeline and leading a product to market.
High emotional intelligence and communication skills required to manage up to executive level stakeholders. You act as the "single source of truth," filtering noise and delivering clarity.
Demonstrated ability to influence without authority. You can motivate and guide senior functional experts who do not report to you, maintaining momentum even when faced with organizational ambiguity.
Ability to "speak the language" of both the R&D scientists developing the chemistry and the Commercial leaders selling the test. You don't just focus on the science; you focus on the manufacturability and operational scalability of the test.

Nice To Haves

MBA is a strong plus.
Experience navigating FDA Class II/III medical device development (PMA/510k) is highly preferred.

Responsibilities

Cross-Functional Leadership & Accountability Serve as the single point of accountability for the development lifecycle, ensuring the team delivers against the Target Product Profile (TPP) and Product Requirements.
Lead a dedicated Core Team of functional heads (Science, Engineering, Quality, Regulatory, Lab Ops) without direct line authority. You must effectively negotiate priorities, drive consensus among peers with competing incentives, and align disparate groups toward a shared vision.
Ensure the technical and clinical vision defined at the start of the project is consistently understood and executed across all technical sub-teams, preventing scope creep or strategic drift.
Proactively identify and resolve friction between functional groups (e.g., Commercial timelines vs. R&D feasibility). You will serve as the primary mediator, fostering constructive debate to reach rapid, data-driven decisions without needing constant escalation.
Stage-Gate Governance & Strategic Execution Lead the product team through formal Stage-Gate Reviews (Phase Exits). You must possess the executive presence to synthesize complex technical, clinical, and operational data into clear, actionable business narratives for the leadership team.
Proactively identify critical path risks. You will drive difficult trade-off decisions between scope, timeline, and resources, escalating structural blockers to the Executive Leadership Team only when necessary.
Collaborate with functional leadership to ensure appropriate resource allocation, ensuring the project aligns with the broader Tempus portfolio priorities.
Design Control & Operational Scale Champion a development process compliant with Design Control (21 CFR 820) and ISO 13485 standards. You will guide the team through the rigors of LDT, 510(k), or PMA regulatory pathways.
Oversee the critical transition from R&D to Clinical Lab Operations. You will ensure the "order-to-result" workflow is robust, scalable, and ready for commercial volume prior to launch.
Act as the primary link between technical development and the Commercial organization, ensuring that technical milestones translate into market-ready value propositions.