Principal Product Manager

Oracle Oracle · Enterprise · United States

Product Manager for Health Data Intelligence at Oracle Cerner, focusing on developing new products that use advanced analytics and AI to create personalized and predictive health experiences. The role involves defining product strategy, collaborating with cross-functional teams, and ensuring regulatory compliance within the healthcare domain.

What you'd actually do

  1. Serve as a regulatory compliance expert and maintain strong relationships with key clinical teams.
  2. Defining and driving the development of products that align with the company's vision and customer needs.
  3. Conducting market research, gathering customer feedback.
  4. Collaborating with cross-functional teams like Engineering, Data Science, Marketing, Sales, and Business Development to create innovative and customer-centric solutions.
  5. Driving clarify on the Why and What through well written PRDs and effectively prioritizing features.

Skills

Required

  • BS or MS degree in Business, Computer Science, Engineering, or equivalent.
  • 5+ years of experience as a Product Manager or similar role.
  • 3+ years of experience in clinical policy compliance or clinical regulatory/government affairs
  • 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.

Nice to have

  • Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.)
  • 2-3 years of experience in regulatory preferred but may consider quality assurance, research and development/support, engineering, scientific affairs, operations, or related area.
  • Experience collaborating across QA, R&D, Clinical, Labeling, and Operations; may consider strong cross‑functional experience with demonstrable regulatory change leadership
  • Experience with data warehousing, big data, machine learning
  • Experience with building and shipping products on any Cloud platform like OCI, AWS, Azure, GCP
  • Enterprise discernment and market awareness.
  • Healthcare/Health Management background

What the JD emphasized

  • regulatory compliance expert
  • clinical policy compliance
  • clinical regulatory/government affairs
  • EU and other international medical device / drugs / pharma regulations and submissions
  • design controls in medical devices, IVDR, Pharma industries

Other signals

  • AI for personalized and predictive health experiences
  • advanced analytics and AI
  • data-driven decision-making