Data Management
Resume:
Cory L. Pace
Winston-Salem, NC
abkbov@r.postjobfree.com
OVERVIEW:
To obtain an entry level Data Analyst/Collector position in the field of
clinical research. This position will allow me to use my knowledge of data
management task as well as my three years experience in this field to
contribute to the growth of the company.
STRENGTHS and ABILITIES:
. Great leadership, time management, and communication skills
. Creative thinker
. Self motivated, initiative, high level of energy
. Tolerant and flexible to different situations/schedules
. Capable of learning any tasks in a timely manner
Education:
Vance-Granville Community College Louisburg, NC
Major: Computer Information Systems August 2003
Franklinton High School Franklinton, NC
High School Diploma August 1996
Projects/Areas of Expertise:
. Pharmaceutical/CRO industry
. Skilled in discrepancy management
. Expertise in data cleaning and participated in data review listing
. Skilled in the generation of clinical data reports
. Skilled in Electronic Data Capture
. User Acceptance Testing
. InForm (Account Management), Medidata Rave, Clintrial 4.0, Visio
Professional Career Experience:
Duke Clinical Research Institute Durham, NC
Clinical Data Assistant II November 2008 - Present
> Responsible for 1st and 2nd entry and verification of clinical trial
data
> Generate, review queries; update database based on queries; monitor
DCFs and discrepancy management guidelines
> Perform User Acceptance Testing.
> Responsible for importing and exporting of data
> Present project status information to internal team
> Perform tasks associated with database QC and CRF to database audits
and provide input into Corrective Action Plans
> Documentation management
> Data Reporting
> Create and make recommendations for trial specific forms such as CRFs,
DCFs, etc.
> Ensure documents and work instructions are in compliance with SOP
> Perform basic interaction with database systems, including navigation
of the system, data entry, reviewing queries, and printing reports.
> Responsible for reading and understanding eCRFs
> Filing
Statistics and Data Corp. Raleigh, NC
Clinical Data Associate I Oct. 2007 - Oct. 2008
> Conducted entry of clinical trials data in accordance with established
guidelines, study specific protocols and data management plans
> Assisted with user testing and analysis of data entry screens and/or
databases prior to implementation, as needed.
> Accurately documented all problem/errors found while testing
> Participated in internal and external team meetings, as necessary
> Complied with company's data integrity & business ethics requirements
> Performed other related duties incidental to the work described herein
> Assist in the formatting of CRFs
> Enrolled and tracked CRFs
> Processed and routed CRFs per work instructions
> Generated Reports
> Cleaned data based on discrepancies identified on Subject-Detailed,
Verification, Flag, SAE Reconciliation, Missing Page Reports, &
Clinical Listings
> Participated in data review listings
> Performed DCF Updates
> Generated Queries
> Created Test Case Data
> Developed QC/Audit Specifications
> Coordinated and performed study specific training
> Created study specific guidelines (Data Entry Guidelines, CRF
Completion Guidelines)
> Participated in QC Audit (Critical Variable & Post-Close)
Kelly Services Raleigh, NC
Medical Device Assembler Oct. 2006 - Feb. 2007
> Operated machines
> Performed Inspections
> Assembled quality medical devices/products
> Handled a limited number of chemical, company products, and cleaning
solvents.
> Cleaned fill room and device assembly equipment according to S.O.P.s
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