Clinical Data Analyst

V-Soft Consulting is currently hiring for a Clinical Data Analyst for our premier client in Chicago, IL. This is a contract position in the healthcare industry.

The Analyst will support the research, clinical, quality improvement, and business data analysis needs of our client. The Analyst will assist clinical faculty and Principal Investigators to identify and gather necessary data that span operational through research needs and will build data sources to permit queries. The analyst will have a direct reporting relationship to the Director of Clinical Research Analytics. Exemplifies our client’s mission, vision and values and acts in accordance with policies and procedures.

WHAT YOU’LL NEED:

Education and Experience ?

• Master's degree in information science, computer science, epidemiology, biostatistics, or equivalent technical experience.
• Strong analytic, issue resolution, and facilitation skills.
• Demonstrated proficiency writing SQL stored procedures or queries.
• Able to present complex information in an understandable and compelling manner.
• Able to prioritize and multi-task to manage expectations of multiple stakeholders.
• Able to deliver high quality, timely work product with significant autonomy.
• Effectively adapts to rapid changes in project or data requirements and changing directions.
• Strong written and verbal communication.
• Effective interpersonal and teamwork skills.
• Expertise with data and analytics tools.
• Experience querying and analyzing data with SQL programming language or equivalent tools.

Preferred Job Qualifications:

• Experience with healthcare information technology in the hospital setting
• Experience with Forte OnCore Enterprise Research Clinical Trials Management System (CTMS)
• Experience with Huron (Click) Research Suite
• Experience in building or working with data marts that consolidate data from multiple applications
• Experience with Epic EMR (Epic Cogito Certification desired)
• Experience querying, analyzing, and visualizing data in both relational databases and data warehouses with SQL or tools such as python or Tableau
• Experience in statistical software, such as SAS, R, or python
• Experience with regulatory compliance for and governance of clinical research, including HIPAA, the Common Rule (45 CFR 46), and Institutional Review Boards (IRBs)

WHAT YOU’LL DO:

Job Responsibilities ?

• Supports projects that leverage data collected from a variety of sources to aid in the administration of clinical trials. Applications include:
• Forte OnCore Enterprise Research Clinical Trials Management System (CTMS)
• Huron (Click) Research Suite
• Epic
• Gather data requirements from administrators and researchers.
• Contributes to the design of studies and identifies study cohorts.
• Works with clinical experts and Information Systems to determine feasibility, timelines, and costs of data requests.
• Uses software tools and data sources to develop queries, reports, and visualizations.
• Creates and maintains data sources, including custom data marts, to support research.
• Member of the Information Systems team at our client.

EMAIL ME: [email protected]