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Job Requirements of Global Project Manager:
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Employment Type:
Full-Time
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Location:
Tucson, AZ (Onsite)
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Global Project Manager
Tailored Management Services Inc
Tucson, AZ (Onsite)
Full-Time
Job Title: Global Project Manager
Location: 1910 East Innovation Park Drive, Tucson, AZ 85755
Duration: 12+ month contract (potential extension or permanent hire)
Pay Rate: $58.00/hour
Benefits: Weekly pay; medical, dental, and vision coverage
Work Arrangement: Hybrid (2 days/week onsite in Tucson, AZ); approx. 5% travel
Schedule: Monday – Friday, 1st shift
About Us:
At Roche, our vision is a healthier future for all. We're passionate about advancing science and innovating to ensure access to healthcare now and for future generations. We strive to create more moments for people to spend with those they love.
Role Overview:
As a member of the Project Management Chapter (PMC), the Global Project Manager (GPM) is pivotal to advancing product delivery for Roche. You’ll manage and oversee projects of varying complexity, guiding them from concept to completion. This includes developing work plans, schedules, budgets, resource strategies, and reporting on progress. Acting as a trusted advisor, you’ll translate organizational needs into actionable projects, driving efficiency and agility across our portfolio.
Key Responsibilities:
Who You Are:
Preferred Qualifications:
Location: 1910 East Innovation Park Drive, Tucson, AZ 85755
Duration: 12+ month contract (potential extension or permanent hire)
Pay Rate: $58.00/hour
Benefits: Weekly pay; medical, dental, and vision coverage
Work Arrangement: Hybrid (2 days/week onsite in Tucson, AZ); approx. 5% travel
Schedule: Monday – Friday, 1st shift
About Us:
At Roche, our vision is a healthier future for all. We're passionate about advancing science and innovating to ensure access to healthcare now and for future generations. We strive to create more moments for people to spend with those they love.
Role Overview:
As a member of the Project Management Chapter (PMC), the Global Project Manager (GPM) is pivotal to advancing product delivery for Roche. You’ll manage and oversee projects of varying complexity, guiding them from concept to completion. This includes developing work plans, schedules, budgets, resource strategies, and reporting on progress. Acting as a trusted advisor, you’ll translate organizational needs into actionable projects, driving efficiency and agility across our portfolio.
Key Responsibilities:
- Lead innovative Companion Diagnostics projects, collaborating with internal teams and external Pharma partners.
- Own and coordinate project/program structures, overseeing development, timelines, resources, budgets, and communication.
- Develop integrated project plans, manage dependencies, and ensure resources align with objectives and budgets.
- Ensure quality and deliverable integrity in complex projects, focusing on risk management, critical path analysis, scenario planning, and cost control.
- Proactively identify risks, gaps, and bottlenecks; challenge assumptions; and suggest creative solutions to keep projects on track.
- Consistently apply project management processes, lead milestone and capacity reviews, and implement best practices to foster continuous improvement.
- Select and apply the most suitable project methodologies, including Agile practices where appropriate; coach teams in both Agile and traditional methods.
- Facilitate meetings, encourage knowledge sharing, and enhance team effectiveness.
- Define, track, and report on KPIs, metrics, OKRs, and outcome-based project goals.
- Advise teams and the broader organization on holistic planning, risk management, scenario modeling, and critical path analysis.
- Serve as the central point of contact for project/program data and governance.
- Manage team information for internal and portfolio-level decision-making.
- Act as Agile Program Manager (as per Scaled Agile Framework - SAFe) when needed.
Who You Are:
- Proficient with project management tools including Planisware, MS Office, G-Suite, Trello, LucidChart, Smartsheet, Jira, Azure DevOps, etc.
- Skilled in problem-solving, critical thinking, and analyzing complex data to drive improvement.
- Proven experience managing highly complex product development projects from concept to commercialization, especially in regulated industries.
- Strong interpersonal, influence, and communication skills; adept at collaborating and driving proactive decision-making with stakeholders.
- Solid understanding of Design Control, Phased Development, and healthcare quality/regulatory compliance.
- Strategic, tactical, and analytical thinker with a value-driven mindset.
- Capable of escalating issues and influencing management decisions in project execution and resource allocation.
- Bachelor's degree in science, engineering, or a related field (required).
- 4+ years project management experience in diagnostics, medical devices, health sciences, pharma, or biotech industries; experience in other regulated industries also considered.
- At least 1 year of experience in clinical biomarker or IVD development, companion diagnostic development, analytical/clinical validation and regulatory submissions, or instrument development/program management.
- At least 1 year of experience working in a regulated environment (e.g., FDA 21 CFR part 820, ISO 13485, ISO 9001).
Preferred Qualifications:
- Master’s degree in science, engineering, or business.
- Experience with Agile development principles and methodologies.
- PMP and/or SAFe certification.
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