Sr. Microsoft BI Architect in Indianapolis IN

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Sr. Microsoft BI Architect

Location: Indianapolis IN

LOA: 6 month contract, potential for extension

 

Interview Process: Candidates will interview with 4 internal managers and we would like to start scheduling interview ASAP

 

 

Project Overview

The Clinical Laboratory Results Modernization (CLRM) program is a series of related efforts that aim to:

• Consume, standardize, and store all of Lilly's clinical trial laboratory and diagnostics results and sample logistics data into one data warehouse where they will be integrated with other relevant clinical trial data and provided to the appropriate downstream systems.
• Take advantage of efficiencies enabled by the use of industry standards (e.g. CDISC Lab Data Model).
• Improve the quality of laboratory and diagnostics results sent to Lilly by its third party central vendors.
• Support Lilly's Clinical Laboratory Operations (CLO) business processes by providing central vendors with appropriate visibility into clinical trial data as it is being collected.
• Reduce costs by enabling the retirement of some clinical trial lab and diagnostic results systems.

CLRM Release 1 will focus on discreet lab, ECG reading and imaging reading results only.  The scope of work for this engagement includes:

• Creating a reporting environment for CLRM R1 utilizing Microsoft BI technologies
• Creating 15 pre-defined reports, as well as providing ad hoc reporting capabilities
• Providing input into the documentation, testing, and training processes

 

Position Overview

The Sr. Microsoft BI Architect will be responsible for data modeling, cube design, application development, technical product assistance and tuning to meet customer performance and functional requirements:

• Create and develop SQL Server Integration Services (SSIS) packages
• Create and design SQL data models Server Analysis Services (SSAS) cubes
• Work with team to provide access to reports and data through SharePoint 2013
• Act as the subject matter expert for the input, analysis, and reporting of clinical trials & diagnostic data in a secure environment
• Provide input into the development or modification of data structures and schemas related to clinical trials data using CDISC standards
• Interact with business frequently to determine needs and project directions
• Advise business on best practices
• Perform cube design, development, and delivery estimation-provide work break down structures
• Provide content & collateral for user training and solution maintenance

 

Technical Skills

Must Have: 

• Microsoft BI Experience including:  Microsoft SQL Server, MS SQL Server Integration Services (SSIS), MS SQL data models Server Analysis Services (SSAS)
• Data warehouse design & development
• Data modeling & multi-dimensional cube development
• Experience integrating multiple data sources
• Reporting secured, clinical data in a controlled environment, including blinded data
• Experience with CDISC Lab Data Model
• Pharma/clinical experience is key

Nice to Have: 

• MS SQL Server Reporting Services (SSRS)
• SharePoint 2013 Development
• Oracle DB
• Planisware

 

Non-Technical Skills

Must Have: 

• BI Consulting Practice Experience
• Pharmaceutical Industry Experience
• Self-starter, independently motivated, team-player, group collaborator
• Excellent verbal & written communication skills
• Willingness & ability to create and share ideas in a team environment

 

Nice to Have: 

• Diagnostic Laboratory Experience
• Team Leadership
• Agile development
• SDLC

 

  

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Thanks & Regards,

Tarun Vohra

Sr. Team Lead

Sage Group Consulting, Inc.

3400 Highway 35, Suite # 9, Hazlet, NJ 07730

Direct Phone: 732-479-1329

Office: 732-767-0010 EXT:210

Fax: 732-479-1329

Email    : tvohra@sagetl.com

Website : www.sageci.com

Yahoo IM : tarun.vohra

Gtalk IM : tarun.vohra84

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