Oversees and strategizes the data analytics needs of the organization, including analysis of population health metrics, network clinical, financial, utilization, and patient satisfaction in support of the optimization of Dignity Health MSO's performance relative to value-based contracts. Leads a team to provide and strategize results for hands on data science and analytics functions for Dignity Health MSO leadership. Collaborates with Dignity Health MSO leadership and provider network to achieve organizational goals.
Provide oversight development of datasets ,Generate and/or review of SDTM mapping specifications, annotated CRFs, ADaM specifications, define.XML documents and reviewers’ guides per CDISC and FDA specifications and guidelines. Accountable for oversight of statistical programming deliverables for inhouse and outsourced projects.
In this role on the Healthcare Data Analytics team, you will play a pivotal role in analyzing and interpreting complex healthcare data to support strategic decision-making and improve population health outcomes. You will work closely with Interwell Health colleagues and stakeholders to understand analytical needs, develop insights that drive healthcare initiatives, optimize resource allocation, and enhance patient care.
AbbVie Clinical Data Strategy and Operations is a best-in-class team responsible for generating business value from clinical trials data through execution and innovation. This role ensures successful delivery of program- and study-level accountabilities, developing a deep understanding of clinical technology capabilities and data flow. Responsibilities include supporting technology delivery, tracking timelines, developing reports, collaborating with stakeholders, and maintaining technical knowledge of clinical data systems.
As a Data Analyst, you will play a critical role in delivering first-class evaluations and measurement options based on data to support client decision making in a reliable and efficient manner. Investing in proper data analysis at the onset of a project is key for successful delivery overall.
As a SAS Programmer you execute studies generating real-world evidence to evaluate drug safety, effectiveness and value, in a full-time temporary position for a fixed-term contract. You will develop, validate, and maintain SAS and SQL programs to support statistical analysis of real-world data. Collaborate with epidemiologists, data scientists, statisticians, and clinical researchers to define programming requirements and ensure accurate and reproducible analyses.
Lead and oversee complex statistical analyses, provide high-level strategic recommendations, and guide junior analysts in the execution of observational research. This leadership position combines technical expertise with client-facing responsibilities, allowing the successful candidate to influence key decisions within our client’s RWE and cross-functional teams.