Senior Project Leader
$130,700–$261,300 year
On-siteAlameda, California, United States
Job Summary
Lead strategy, prioritization, and delivery of complex digital health initiatives from concept through commercialization while managing cross-functional teams across R&D, Commercial, Clinical, and Regulatory functions. Define program roadmaps, business cases, and release strategies; drive portfolio prioritization; and lead product launches and geographic expansion efforts. Mentor Project Leaders, establish success metrics, and proactively mitigate risks to ensure execution excellence and strategic alignment. Present complex information to senior stakeholders and champion PMO best practices to enhance delivery performance.
Required Qualifications
- Bachelor's degree
- 5+ years of experience leading product development, program management, or strategic initiatives within the medical device, digital health, or healthcare industry
- Proven track record of successfully leading complex, cross-functional programs from concept through launch, preferably involving digital products
- Strong stakeholder management, influencing, and negotiation skills, with the ability to build alignment and resolve conflict across functions, organizations, and external partners
- Exceptional communication, presentation, and storytelling skills, including the ability to create compelling presentations and effectively communicate with stakeholders at all levels
- Analytical and problem-solving skills, with the ability to synthesize information from multiple sources, balance competing priorities, and drive resolution of complex cross-functional issues
- Strategic thinker with the ability to navigate ambiguity and drive results
- Bachelor's degree, English major preferred
Desired Qualifications
- Experience leading digital health, connected device, mobile application, or software-enabled healthcare products
- Strong organizational and time management skills, with a track record of delivering high-quality work on schedule
- Highly motivated, goal-oriented, and able to manage multiple priorities simultaneously
- Comfortable operating in a fast-paced environment with competing deadlines
- Working knowledge of medical device regulations and standards, including FDA, ISO, and QSR Design Controls
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