Senior Clinical Data Analyst Resume

PROFESSIONAL EXPERIENCE

Confidential

Senior Clinical Data Analyst

Responsibilities:

Create datasets using Oracle SQL developer and SAS for submission to FDA and to assist clinical teams with the enforcement of data integrity
Evaluate use of Oracle BI Publisher for use as reporting tool by Clinical Data Management
Work with Clinical Trial teams to design case report forms, edit check specifications and report specifications
Designed SAS code to automate the gathering of clinical data for biostatisticians
Automated creation of Excel spreadsheets used by clinical teams to analyze their data
Work with Clinical Trial Project Managers to update Data Management Plans

Confidential

Senior Data Analyst

Responsibilities:

Designed IT executive dashboard by collecting requirements from various groups, designing SQL Server databases to house data, designing ETL with SSIS and creating reports with SSRS
Project management reporting for IT project management group
WebEx and telephone invoice reporting
Redesign of ETL process that exports data from a time tracking system to a dimensional datamart; also served as project manager, coordinating efforts of DBA’s, Systems personnel and financial controller to upgrade the time tracking system
Documentation of dataflow into Oracle financial system from various sources
Project management reporting for Oracle financial projects
Work with Sales Analysis department to create a reporting database which merged sales, financial and Dunn and Bradstreet corporate data
Work with vendor and internal IT staff to build ETL feed for externally hosted training system

Confidential

Senior Report Writer/Developer

Responsibilities:

Worked on Clinical Data Management team to support clinical trial personnel by designing reports to analyze and monitor status of cardiac device trials
Validated reports from other programmers and bio - statisticians for submission to FDA and other regulatory bodies using Clindex Clinical Trial software
Supported lead clinical systems programmer in his development of adverse event tracking tool for clinical trial personnel in PowerBuilder
Occasionally supported clinical forms developers by testing new clinical interface screens as well as creating and documenting test cases
Worked with lead clinical systems programmer to construct and support device accountability interfaces between Clindex and SAP; also researched and corrected device accountability data issues
Worked with clinical personnel to adjust Oracle/Agile work flow system so that reports received appropriate approval depending on their importance
Developed report training documentation and co-taught training classes for clinical personnel so that they could make efficient use of the reporting systems.