Global Project Manager – Companion Diagnostics (CDx)
Location: Tucson, Arizona, United States
Work Mode: Hybrid (On-site ~2 days/week, Oro Valley, AZ campus)
Job Type: Full-Time | Permanent
Category: Research & Development
Sub-Category: Research
Industry: Diagnostics / Medical Devices / Pharmaceuticals / Biotech
Company: Roche
Job Level: Individual Contributor
Experience Required: 4–6+ Years
Job ID: 202601-100336
Posted Date: 01 September 2026
Job Overview
Roche is seeking a highly skilled Global Project Manager (GPM) to lead and deliver complex global projects within Companion Diagnostics (CDx) product development and product lifecycle management. As part of the Project Management Chapter, this role is responsible for driving projects from concept through commercialization while ensuring optimized value delivery, regulatory compliance, and cross-functional alignment.
The Global Project Manager serves as a trusted advisor, enabling efficient portfolio execution and supporting rapid response to evolving business and regulatory needs across global teams.
About Roche
Roche is a global leader in diagnostics and pharmaceuticals, dedicated to advancing science and improving patient outcomes worldwide. With more than 100,000 employees globally, Roche fosters a culture of inclusion, innovation, and accountability while delivering life-changing diagnostic and therapeutic solutions.
Key Responsibilities
Global Project and Program Leadership
Own and manage end-to-end project structures for Companion Diagnostics product development and product care activities.
Develop, coordinate, and maintain integrated project plans, including timelines, dependencies, resources, budgets, and risk mitigation strategies.
Drive robust project execution covering risk management, critical path analysis, scenario planning, budget control, and cost tracking.
Serve as the single point of control for project and program data across functions.
Governance, Metrics, and Reporting
Lead preparation and execution for milestone reviews, capacity reviews (cQCR, SCR, fQCR), and other governance forums.
Establish, track, and report Key Performance Indicators (KPIs), Objectives and Key Results (OKRs), and Outcome-Based Planning (OBP) metrics.
Provide portfolio-level planning data to support scenario analysis and executive decision-making.
Agile and Hybrid Project Management
Select and apply appropriate project management methodologies, including Agile, hybrid Agile, and traditional approaches.
Act as an Agile Program Manager (SAFe framework) where applicable.
Coach and guide teams on Agile practices while integrating non-Agile techniques for external partners and regulated functions.
Promote continuous improvement by sharing best practices across project and program teams.
Stakeholder Engagement and Risk Management
Lead cross-functional project team meetings and foster collaboration across R&D, Regulatory, Quality, Clinical, and external partners.
Identify risks, gaps, and bottlenecks impacting scope, budget, or timelines, and proactively implement corrective actions.
Communicate project status, risks, and mitigation strategies clearly and effectively to stakeholders at all levels.
Required Qualifications
Education
Bachelor’s degree, preferably in Life Sciences, Engineering, or a related discipline.
Experience
Minimum 4 years of experience in full lifecycle project management within diagnostics, medical devices, pharmaceuticals, biotech, or engineering industries.
At least 1 year of experience in one or more of the following areas:
Companion Diagnostics or In Vitro Diagnostic (IVD) development
Clinical biomarkers
Analytical and clinical validation
Regulatory submissions
Instrument or systems development
1 year of experience in a regulated environment, such as FDA 21 CFR Part 820, ISO 13485, or ISO 9001.
1 year of experience collaborating with external partners, managing timelines, deliverables, and performance expectations.
Proven experience creating and maintaining complex project schedules using tools such as MS Project, Smartsheet, or equivalent platforms.
Preferred Qualifications
Master’s degree in Life Sciences or related field with 6+ years of project management, engineering, or business experience in regulated industries.
Alternatively, a PhD with 3+ years of project management experience in diagnostics, medical devices, pharma, or biotech.
3+ years of experience in CDx, IVD development, analytical/clinical validation, regulatory submissions, or instrument development.
Hands-on experience with Agile and hybrid delivery models using tools such as JIRA, Azure DevOps (ADO), or similar platforms to manage global programs.
Location and Compensation
This is a hybrid role requiring on-site presence approximately two days per week in Oro Valley, Arizona.
Relocation assistance is not available for this position.
Expected salary range for Tucson, AZ: USD 87,900 – 163,200, based on experience, qualifications, and geographic location.
Eligibility for Roche’s comprehensive benefits package and performance-based incentives.
Why Join Roche
Lead global Companion Diagnostics programs with high patient impact
Work in a collaborative, innovation-driven R&D environment
Apply advanced project management and Agile methodologies at scale
Contribute directly to life-changing diagnostic technologies
Equal Opportunity Statement
Roche is an Equal Opportunity Employer. Employment decisions are based on merit, qualifications, and competence, without discrimination, in accordance with applicable laws. Reasonable accommodations are available throughout the application process.
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