Clinical Information Analyst (on-site)

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career you dream of
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists

The Clinical Information Analyst will work out of our Santa Clara, CA location and is responsible for the development and optimization of reporting solutions which support and advance data-driven problem solving in the conduct of clinical trials. This individual will work under Good Clinical Practices, Good Clinical Data Management Practices, and other FDA regulations and guidelines, and must demonstrate solid oral and written communication skills and analytical/problem-solving skills at various levels of the organization. 

• Partner with shared service functions such as Site Management, Study Management, Data Review, Safety, etc. to gather operational, analytical, and study-specific reporting requirements.
• Develop elegant and efficient reporting solutions (primarily SQL queries in Oracle RDBMS and Power BI visualizations) to meet reporting requirements.
• Support ongoing maintenance and enhancement of reporting portfolio.
• Peer Review and QC of products.
• Support and train end-users of reporting portfolio
• Support the development and standardization of reporting conventions.

• Bachelor’s degree OR an equivalent combination of education and work experience
• Minimum 2 years’ related experience with a good understanding of specified functional area.
• Good knowledge and application of business concepts, procedures and practices.

• Bachelor’s degree in Business Administration, Data Science, Statistics, or Life Sciences
• Strong clinical research and/or data analytics experience.
• Strong preference for experience with Oracle RDBMS, Power BI, SSRS;
• Experience with SQL, Python, Vega/Vega-Lite
• Experience with Clindex/Tableau is a plus
• Exceptional interpersonal and rapport-building skills, and excellent analytical/problem-solving skills at various levels of the organization. 
• Must be able to effectively manage multiple projects and timelines.
• Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.

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