
Director, Program Management
Posted Aug 8

Posted Aug 8
This is a fully remote position, open to applicants in United States.
• Oversee the planning, implementation, and completion of strategic projects across various workstreams, such as revenue cycle management, product development, laboratory enhancements, and digital platforms.
• Enhance PMO organizational capabilities and establish best practices, tools, and discipline in program management.
• Collaborate with leaders from Product, Clinical, Lab Operations, Informatics, Software Engineering, Regulatory, and Quality to outline objectives, priorities, and success metrics.
• Lead program governance through KPIs, timelines, milestones, budgets, and reporting frameworks.
• Track progress and make necessary adjustments to programs.
• Organize steering committee and stakeholder meetings to provide status updates, assess risks, and request decisions.
• Communicate program progress to executive leadership, including the CEO, via structured updates, dashboards, and strategic reviews.
• Identify, evaluate, and mitigate risks; escalate issues to ensure timelines and objectives are met.
• Manage dependencies and resource allocation across teams effectively.
• Ensure adherence to CLIA, CAP, HIPAA, Part 11, and other relevant healthcare regulations.
• Conduct post-implementation reviews and integrate lessons learned into future projects.
• Offer guidance, mentorship, and leadership to project teams.
• Perform additional duties as assigned and adhere to company policies, procedures, and regulatory standards.
• Bachelor’s degree in a relevant discipline such as Life Sciences, Health Administration, Business, or Engineering.
• Over 10 years of experience in new product development, program management, and/or portfolio management within the biotech, life sciences, or diagnostics sectors.
• At least 8 years of experience in Program Management or Portfolio Management.
• A minimum of 3 years in a leadership role overseeing teams.
• Proven experience managing large-scale, cross-functional programs that involve complex systems integration and business process transformation.
• Strong knowledge of laboratory workflows, clinical testing processes, and healthcare regulatory compliance.
• Proficient in project and portfolio management tools such as Microsoft Project, Smartsheet, and PKIT.
• Outstanding communication and stakeholder engagement abilities.
• Strong executive-level communication skills.
• An equivalent combination of education and experience may be considered.
• Preferred experience in regulated laboratory settings, including diagnostics, genomics, or molecular testing.
• PMP, PgMP, SAFe Agilist, or an equivalent certification is preferred.
• Experience in supporting the development or commercialization of clinical laboratory tests is preferred.
• Remote work arrangement.
• Periodic travel may be necessary based on business needs.
• Commitment to an equal opportunity and inclusive workplace.
• Accommodation support available during the application process.
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