Laboratory Project Manager (on-site)

Rocky Mountain LaboratoriesTempe, AZ
16h$75,000 - $85,000Onsite

About The Position

Clinical Laboratory Project Manager Rocky Mountain Laboratories – Tempe, AZ About Us Rocky Mountain Laboratories is a clinical laboratory providing comprehensive laboratory services. We are dedicated to delivering accurate and timely diagnostic information and are committed to improving healthcare outcomes through cutting-edge technology and a customer-focused approach. Position The Clinical Laboratory Project Manager leads and coordinates cross-functional initiatives across molecular diagnostics, toxicology, clinical chemistry, and laboratory operations. This role exists to bring structure, visibility, and execution discipline to a growing clinical laboratory environment. As Rocky Mountain Laboratories continues to expand assays, instrumentation, and operational complexity, this position plays a critical role in ensuring initiatives move forward efficiently, compliantly, and without disruption to patient testing. This role is responsible for translating leadership objectives into structured, actionable project plans; driving workflow optimization initiatives; and ensuring work is completed on time, within scope, and in alignment with regulatory and quality standards. The ideal candidate is highly organized, assertive, and execution-focused. They excel in fast-paced, regulated environments, anticipate obstacles early, and drive clarity, accountability, and follow-through across cross-functional teams. This is not an IT development or construction project management role. This is a hands-on, operations-adjacent project management position embedded within clinical laboratory workflows. Schedule: Monday–Friday, 9:00 a.m. to 5:00 p.m. Occasional flexibility as projects require

Requirements

  • 3–5 years of project management experience, preferably in a clinical laboratory, diagnostics, or regulated healthcare environment
  • Proven ability to manage multiple concurrent projects with shifting deadlines
  • Strong skills in delegation, organization, and cross-functional accountability
  • Excellent written and verbal communication skills, including documentation and meeting facilitation
  • Experience working with lab operations, QA/QC, molecular/clinical scientists, or technical teams
  • Proficiency with project management tools (Gantt charts, trackers, PM platforms, etc.)

Nice To Haves

  • Experience in molecular diagnostics, toxicology, clinical chemistry, or medical laboratory workflows
  • Background in small/mid-sized or high-growth laboratory environments
  • Familiarity with CLIA/CAP requirements, audits, and regulatory compliance
  • Experience with LIMS platforms, workflow automation, or digitally driven lab operations
  • Experience supporting assay implementation, equipment onboarding, or process improvement initiatives
  • PMP, CAPM, Lean, Six Sigma, or similar formal PM training

Responsibilities

  • Project Leadership & Execution Lead laboratory projects from initiation through completion, including timelines, deliverables, dependencies, and progress tracking
  • Translate high-level goals into detailed project plans, workflows, and structured action items
  • Define scope, milestones, success criteria, and cross-functional workstreams
  • Maintain project documentation such as Gantt timelines, action registers, risk logs, and status summaries
  • Support workflow improvement and operational optimization initiatives across clinical laboratory operations
  • Cross-Functional Coordination Drive communication between scientists, lab managers, QA/Compliance, operations, and administrative teams
  • Facilitate cross-department handoffs, ensuring clarity and nothing falls through the cracks
  • Provide consistent progress updates to leadership and project stakeholders
  • Coordinate readiness activities for new assays, equipment onboarding, and LIMS-related workflow changes
  • Quality, Compliance & Technical Support Coordinate verification and validation (V&V) plans, method implementation steps, and related documentation
  • Ensure projects align with CLIA, CAP, and internal quality system expectations
  • Support internal and external audits by preparing and organizing documentation
  • Maintain structured technical documentation, such as design history files, when applicable
  • Accountability & Risk Management Identify risks, bottlenecks, and resource gaps early and propose mitigation strategies
  • Escalate timeline risks, obstacles, or workload imbalances promptly
  • Define, delegate, and track tasks to completion, ensuring accountability across project teams
  • Promote consistent execution and follow-through across departments
  • Operational & Leadership Support Assist leadership with resource planning, prioritization, and capacity balancing
  • Contribute to SOP development, process mapping, and laboratory workflow optimization projects
  • Adapt to shifting timelines while maintaining transparency and structured communication
  • Other duties as assigned

Benefits

  • Health, Dental, and Vision Insurance
  • Paid Time Off (21 days annually for full-time team members)
  • 7 Paid Holidays
  • 401(k) with 50% Company Match up to 6%
  • Health Savings Account (HSA)
  • Short-Term & Long-Term Disability (RML covers 60% of STD premium)
  • Voluntary Life and AD&D Insurance
  • 100% Company-Funded Employee Assistance Program (EAP)
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