Senior Principal Product Manager

Responsibilities

• Serve as a regulatory compliance expert and maintain strong relationships with key clinical teams.
• Deliver executive briefings on regulatory and policy impacts.
• Advise senior leaders on compliance risks and strategy.
• Define and drive the development of products that align with the company's vision and customer needs.
• Conduct market research, gather customer feedback.
• Collaborate with cross-functional teams like Engineering, Data Science, Marketing, Sales, and Business Development to create innovative and customer-centric solutions.
• Drive clarity on the Why and What through well-written PRDs and effectively prioritize features.
• Manage the product development lifecycle and Go-To-Market strategy.
• Identify risks and dependencies and keep stakeholders updated.
• Ensure timely delivery of high-quality products.
• Able to represent Oracle Health Data Intelligence's capabilities at events and conferences and engage with customers.

Qualifications

• BS or MS degree in Business, Computer Science, Engineering, or equivalent.
• 7+ years of experience as a Product Manager or similar role.
• 5+ years of experience in clinical policy compliance or clinical regulatory/government affairs.
• Experience collaborating across QA, R&D, Clinical, Labeling, and Operations; may consider strong cross-functional experience with demonstrable regulatory change leadership.
• Experience with EU and other international medical device / drugs / pharma regulations and submissions.
• Experience with design controls in medical devices, IVDR, Pharma industries.
• Familiarity with agile methodologies and cross-functional teamwork.
• Strong analytical and data-driven decision-making skills.
• Customer-centric approach and understanding of user needs.
• Excellent communication and presentation abilities.
• Critical thinking and product roadmap development.