Lead the entire lifecycle (Concept to Commercialization) of complex, high-impact clinical assay development projects.
Ensure projects align with strategic objectives, adhere to budgetary constraints, and meet all deadlines.
Guide and motivate cross-functional teams throughout the product development process.
Define comprehensive project scope, goals, deliverables, and resource requirements.
Develop detailed project plans, consistent with the Tempus Product Development Process, utilizing approved project management software and tools.
Establish project milestones and maintain strict adherence to timelines and quality standards.
Review, confirm, and ensure the completeness of all project outputs, deliverables, and documentation.
Create accurate project cost estimates, control expenditures, and manage financial reporting.
Proactively identify, analyze, and mitigate potential project risks and resolve critical issues.
Serve as the primary point of contact, delivering regular, clear status reports to senior leadership and project stakeholders.

Bachelor's degree (4 years) in a scientific, clinical, technical, or business field is preferred; an advanced degree is a plus.
5–10+ years of experience in project management, focusing on large-scale, complex initiatives.
Project Management Professional (PMP) certification is highly preferred.
Extensive knowledge of formal project management methodologies and proven experience applying them within the Biotechnology, Clinical Laboratory, or Medical Device industries.
Understanding of CLIA, CAP, GMP, NYSDOH, and FDA regulations and requirements.
Proficiency with project management software (e.g., Smartsheet, MS Project, Jira, Asana) and budget management tools.
Ability to build and maintain effective, trust-based relationships within a diverse, highly results-driven organization.
High attention to detail, ensuring projects are completed on time with a high degree of accuracy and quality.

Senior Program Manager, Product Development

Key skills