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SAGA Diagnosticsposted about 1 month ago
Full-time • Senior
Morrisville, NC
Resume Match Score

About the position

The Director of Project Management will play a critical leadership role in driving the successful launch of PathLight. This individual will lead cross-functional core teams to ensure alignment, execution, and timely delivery of key milestones associated with the LDT product launch. The role requires exceptional project leadership, strategic planning, and collaborative skills to guide teams across clinical, regulatory, quality, operations, and commercial functions.

Responsibilities

  • Lead and facilitate cross-functional core teams to align on goals, timelines, and deliverables for the PathLight LDT product launch.
  • Act as the central point of coordination and accountability for project execution.
  • Develop and maintain comprehensive project plans, including timelines, resource allocation, risk assessment, and mitigation strategies.
  • Track progress against key milestones and ensure proactive issue resolution.
  • Collaborate closely with internal stakeholders, including R&D, clinical, regulatory, quality, manufacturing, and commercial teams, to ensure seamless integration and execution of launch activities.
  • Communicate project status, risks, and opportunities to executive leadership and key stakeholders.
  • Ensure project activities align with applicable regulatory and quality standards under 21 CFR Part 820 and other global requirements.
  • Demonstrate expertise in launching products in regulated environments, including familiarity with IUO and IVD launches, labeling requirements, and post-market surveillance.
  • Lead launch activities for the US market while planning for and supporting global expansion, including the EU, Japan, and Rest of World (ROW).
  • Collaborate with regional teams to ensure compliance with local regulatory and market-specific requirements.
  • Ensure alignment with the overall corporate strategy, including regulatory compliance, quality standards, and commercial objectives.
  • Support preparation for CLIA, CAP, and NYS DoH compliance, as required for PathLight’s launch.
  • Identify opportunities for operational improvements within the project management function and cross-functional workflows.
  • Implement best practices for project management to enhance efficiency and collaboration.

Requirements

  • Bachelor’s degree in a relevant field (e.g., life sciences, engineering, business); advanced degree preferred.
  • 10+ years of experience in project management within the life sciences, diagnostics, or biopharmaceutical industry.
  • Proven track record of leading cross-functional teams in the successful launch of diagnostic products or LDTs in a regulated environment.
  • Strong understanding of clinical, regulatory, and quality requirements for LDTs, including familiarity with IUO and IVD launches and 21 CFR Part 820.
  • Experience with global product launches, including in the EU, Japan, and ROW, as well as understanding of regional regulatory and market requirements.
  • Familiarity with CLIA, CAP, and NYS DoH compliance, as well as FDA regulations for diagnostic products.
  • Exceptional organizational, communication, and leadership skills.
  • PMP or equivalent certification preferred.

Benefits

  • Competitive salary
  • Dynamic startup culture with regular team events

Job Keywords

Hard Skills
  • Best Practice Implementation
  • Corporate Strategy
  • Executive Leadership
  • Project Communications
  • Project Management
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