Key skills
Clinical policy complianceClinical regulatory affairsRegulatory affairs certification (RAC)Medical device regulationsIVDRPharma industry regulationsAgile methodologiesData warehousingMachine learningCloud platforms OCICloud platforms AWSCloud platforms AzureCloud platforms GCPProduct roadmap developmentGoRAIMachine LearningData WarehousingAnalyticsAWSAzureGCPOracleAgileLeadershipCommunicationCritical ThinkingSales
About this role
Oracle is leading the way in AI and cloud solutions that impact billions of lives. As a product manager for Health Data Intelligence, you will spearhead the development of innovative products that utilize advanced analytics and AI to enhance health experiences for customers.
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
Requirements:
- 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
- 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
- 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