We pride ourselves on revolutionizing the way health data is captured, analyzed, and transformed into actionable insights. With Oracle Cerner's innovative technology, we seamlessly package this valuable information into a range of services and solutions that integrate seamlessly into your favorite analytics tools, EHR applications like Millennium, and even new, groundbreaking applications developed in collaboration with our esteemed partners. Come join a new era of comprehensive health analytics, where data-driven decision-making meets the power of innovation, all at your fingertips. Experience the future of healthcare with us today!
As a product manager for Health Data Intelligence, you will spearhead the development of brand new products. These innovative solutions apply advanced analytics and AI to empower our customers to create highly personalized and predictive health experiences. These experiences range from efficiently analyzing and acting upon the operational health of hospital systems or entire nations of citizens to recommending tailored care plans for specific patients, thereby effectively managing chronic diseases.
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.
- Defining and driving the development of products that align with the company's vision and customer needs.
- Conducting market research, gathering customer feedback.
- Collaborating with cross-functional teams like Engineering, Data Science, Marketing, Sales, and Business Development to create innovative and customer-centric solutions.
- Driving clarify on the Why and What through well written PRDs and effectively prioritizing features.
- Managing the product development lifecycle and Go-To-Market strategy.
- Identify risks and dependencies and keep stake holders updated.
- Ensuring timely delivery of high-quality products.
- Ability to represent Oracle Health Data Intelligence's capabilities at events and conferences and engaging with customers.
Internal Responsibilities
Basic Qualifications:
- 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
- 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 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.
Preferred Qualifications:
- 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
External Responsibilities
Basic Qualifications:
- 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
- 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 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.
Preferred Qualifications:
- 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
