Job Description

*The Clinical Information Analyst will work out of our Maple Grove, MN 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.

*Required Qualifications 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. Experience in data collection and best practices for clinical trials. Good knowledge and application of business concepts, procedures, and practices. Preferred Qualifications 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 PowerBI/Tableau is a plus Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. Must be able to effectively manage multiple projects and timelines

Years Experience: 5+ years related work experience

Skills: Strong analytical and communication skills (oral and written), sound judgment, effective in a team environment (colleagues, software developers and/or customers). Proficiency in Microsoft applications required.

Education: Bachelors Degree in Computer Science, Information Systems or similar discipline including Biomedical Engineering, Electrical Engineering or Healthcare Informatics preferred.

Duties: Define, configure and test core laboratory/hospital software solutions for designs of intermediate or moderate complexity. Develop use cases, requirements and specifications for new and existing system design. Evaluates and defines product changes to resolve customer issues and provide input on new functionality of moderate complexity projects. May leads technical discussions. Participates in investigations to timely determine root causes for moderately complex issues that may cross multiple products. Performs software installation and configuration; test laboratory workflows; creation and maintenance of business rules; verification of system and instrument interfaces Generates input to service personnel Reviews technical risks and take appropriate action. Reviews and provides input into risk management documentation including FMEA and risk analyses.

Exempt/Non Exempt: Non-exempt

Pay ranges between $40-44/hr based on expereince 

Job Tags

Contract work, Work experience placement,

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