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Oracle Sr. Clinical Data Management Analyst in San Diego, California

Lead a team that acts as the central resource and driving force for the design, process, manufacturing, test, quality and marketing of product(s) as they move from conception to distribution. Organize interdepartmental activities ensuring completion of the project/product on schedule and within budget.

As a member of the product development division, you will analyze and integrate external customer specifications. Suggest and justify product directions and specifications. Specify, design and implement moderate changes to existing software architecture. Build new products and development tools. Build and execute unit tests and unit test plans. Review integration and regression test plans created by QA. Communicate with QA and porting engineering to discuss major changes to functionality.

Work is non-routine and very complex, involving the application of advanced technical/business skills in area of specialization. Leading contributor individually and as a team member, providing direction and mentoring to others. BS or MS degree or equivalent experience relevant to functional area. 7 years of software engineering or related experience.

Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans status or any other characteristic protected by law.

Seeking a Clinical Data Management (CDM) subject matter expert to join the Oracle Health Sciences Global Business Unit (HSGBU) product strategy team. You will work closely with the Life Sciences community to analyze needs, gather requirements, and provide direction for various solutions, frequently operating at the leading edge of technology. You will help drive strategy and direction for current and new products/services/processes related to CDM, as well as contribute to the development of new business opportunities and partner relationships to grow the pipeline. You will build and maintain a network and stay up to date on specific industry and product topics, as well as lead and participate in internal and industry projects/initiatives to stay current on trends, provide thought leadership, and explore further CDM opportunities and innovations.

Key Responsibilities:

  • Lead and participate in internal/external projects and initiatives (e.g., CDISC 360).

  • Contribute to product documentation, best practices, and training materials.

  • Obtain and analyze raw data from multiple sources (e.g., clinicaltrials.gov).

  • Lead and participate in pilots and proofs of concept.

  • Develop processes and scripts to automate routine activities.

  • Contribute to solution architecture, standards, and procedures.

  • Provide input and training on industry trends, solutions, and product positioning.

  • Contribute to solution strategy and direction for CDM-related solutions and for customers considering or already utilizing these solutions.

  • Identify opportunities to develop processes and solutions to address complex business needs.

  • Participate in strategic council meetings and events.

  • Conduct competitor analyses.

  • Support planning and provide thought leadership in marketing events and external forums.

  • Build and maintain a network and stay up-to-date on industry and product topics.

  • Establish key relationships with customers and partners.

  • Understand the drivers and challenges of the business and translate them into requirements.

  • Work with customers, prospects, and partners to provide thought leadership and direction for various solutions.

  • Contribute to and participate in user focus group meetings.

  • Support development of new business opportunities and partner relationships to grow pipeline.

  • Other duties as requested or assigned.

Competencies:

  • Bachelor s degree

  • 5 years of experience in Clinical Data Management and/or Clinical Programming

  • Experience with clinical data standards (esp. SDTM) and metadata management preferred

  • Experience with SAS, R, and/or PL/SQL

  • Experience with EDC, CRF annotation, database specifications, and listings review

  • Analytics experience preferred

  • Ability to communicate clearly and concisely at all levels internally, as well as with partners and customers

  • Demonstrates curiosity in both data and business aspects

  • Ability to quickly learn new processes and tools to accomplish goals effectively and efficiently

  • Regarded as an expert in the technical/functional area and reaches out to other expert resources when appropriate

  • Thrives in a dynamic work environment and is able to handle day-to-day work challenges confidently, is willing and able to adjust to multiple demands and shifting priorities, and demonstrates resilience and flexibility

  • Makes timely, cost effective and sound decisions, even under conditions of uncertainty

  • Able to gather and apply input from multiple teams and/or individuals on deliverables

  • Sets high standards of performance, pursues aggressive goals, and works efficiently to achieve them

  • Emphasizes the need to deliver quality products and/or services and drives self and others for quality and efficiency

Job: *Product Development

Organization: *Oracle

Title: Sr. Clinical Data Management Analyst

Location: United States

Requisition ID: 19000RFP

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