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Tempus AI

Tempus AI

via Remote Rocketship

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Senior Program Manager, Product Development

Anywhere
Full-time
Posted 6/25/2026
Verified Source
Key Skills:
Project Management
Cross-functional Leadership
Budget Management

Compensation

Salary Range

$90K - 130K a year

Responsibilities

Lead and manage complex clinical assay development projects from concept to commercialization.

Requirements

Requires 5-10+ years project management experience, PMP certification preferred, and knowledge of biotech regulatory standards.

Full Description

Job Description: • 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. Requirements: • 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. Benefits: • incentive compensation • restricted stock units • medical and other benefits

This job posting was last updated on 7/1/2026

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