Sr. Manager, PMO

4 days, 15 hours ago
Full-time
Lead
Project and Program Management
Veracyte

Veracyte

Veracyte develops innovative molecular diagnostic tests that provide clinicians with critical insights to enhance cancer diagnosis and treatment, ultimately aiming to improve patient outcomes and reduce healthcare costs.

Pharmaceuticals
251-1K
Founded 2008

Description

  • Develop detailed project plans covering scope, objectives, timelines, and resource allocation for prioritized initiatives.
  • Lead cross-functional project teams across multiple sites and drive stakeholder communication and collaboration.
  • Serve as a leader for assigned programs and projects, including those involving senior-level personnel.
  • Monitor project progress against budget, schedule, resource allocation, issues, risks, and scope changes.
  • Identify, escalate, and address project risks and issues, and implement corrective actions as needed.
  • Work with functional leads to determine resource needs, portfolio capacity, and individual project assignments.
  • Prepare and present project status reports, updates, and milestone reviews to stakeholders and senior management.
  • Maintain complete, current, and properly stored project documentation.
  • Contribute to the design and implementation of project management frameworks and tools.
  • Support continuous improvement and innovation within the PMO and broader organization.
  • Align product and program roadmaps with business goals, portfolio priorities, budgets, and resource plans.

Requirements

  • Minimum 8 years of project management experience in a life-science environment.
  • Experience in diagnostics, genomics, product development, or a similar background is preferred.
  • Bachelor’s or master’s degree in life sciences, biotechnology, engineering, business, or a related field.
  • Proficiency in project management methodologies and tools; Smartsheet experience is ideal.
  • Strong communication, leadership, and interpersonal skills.
  • Extensive experience in product development, particularly with Design Control procedures.
  • Ability to lead people and drive results through cross-functional engagement.
  • Ability to manage change across projects and the broader portfolio.
  • Ability to manage multiple projects simultaneously and prioritize work in a fast-paced environment.
  • Ability to influence in a matrixed organization and present to all levels, including executive leadership.
  • Experience working with cross-functional teams across Product Development, clinical, regulatory, operations, and commercial functions.
  • CAPM, PMP, or equivalent certification is preferred.
  • Remote work designation (#LI-Remote).

Benefits

  • Base salary range of $155,000 to $170,000 USD.
  • Eligibility for additional discretionary bonuses and incentives.
  • Eligibility for restricted stock units.
  • Competitive compensation and benefits package.
  • Remote work environment.
  • Commitment to an inclusive workforce and diverse perspectives.
  • Equal opportunity employment policies.
  • Recognition as a 2024 Certified™ Great Place to Work® in the US and Israel.

Interested in this position?

Apply directly on the company website

Apply Now

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