Data Entry
Resume:
Sherry Mingo
******.*****@*****.***
East Orange, New Jersey 07017
SUMMARY OF QUALIFICATIONS
• Nearly 10 years clinical data management from phase I to IV in pharmaceutical industry
• Effective verbal and written communication skills; highly detail oriented
• Capable of organizing and scheduling management meetings; addressing specific questions
regarding data entry when necessary
• Strong query writting skills for entire CRF booklet/, with detailed experience in relationship
between CRF pages (i.e. AE/SAE relationship to ConMed./Lab pages).
• Team leader with excellent attention to detail and strong communication skills
• Able to work under strict timelines and study specific guidelines
• Trained new employees on various tasks from data entry to data management
• Technical Skills: Oracle clinical, Inform, Clintrials, and Error Remediation; MS Office Suite
EDUCATION
Essex County College- Newark, New Jersey
A.S. in Computer Information Systems, Anticipated Graduation Date 2012 (GPA 3.8)
WORK EXPERIENCE
Spectra Force (Merck Pharmaceutical) Rahway, New Jersey
Data Management Specialist 1/08 - 11/08
• Created and implemented the data entry guidelines for error remediation.
• Served as team leader and liaison between data exchange services department and data
managers in order to ensure accuracy of lab data.
• Identified/reconciled lab data queries, deleted duplicate query entries.
• Responsible for Case Report Form (CRF) print management ensuring that all CRF booklets
are sent to National/International sites (Translated CRF verification for consistency).
Aerotek (Integrium) Bedminster, New Jersey
Clinical Data Coordinator 7/07 - 11/07
• Served on the help desk to assist data managers in locating deviations in their clinical data.
• Wrote queries based on AE/SAE relationship to ConMeds/Prior Med. Hist.
• Facilitated and investigated data clarification forms and made appropriate changes.
• Liaison between investigator sites and clinical data managers.
Clinforce (Mount Sinai & Montifiore Medical Center) NYC & Bronx, New York
Clinical Data Coordinator 10/06 - 4/07
• Transferred data from patient records into CRF pages creating Study Books for Clinical Trials.
• Identified and flagged SAE's for Investigator approval/signature to be reported to SAE
department.
• Researched and produced source documents of specific information upon monitor's request.
• Accountable for accurate modifications of lab values from patient hospital files to the
parameters of the study protocol.
WORK HISTORY CONT'D
Assistant Data Manager, Med focus (Novartis), East Hanover, New Jersey, 10/05 - 4/06
Clinical Data Coordinator, Smith Hanley (Pfizer), NYC, New York, 9/03 - 7/04
Clinical Data Associate, Kelly Services (Ingenix), Basking Ridge, New Jersey, 1/02 - 12/02
Data Management Associate, Kelly Services (Novartis), East Hanover, New Jersey, 9/01 - 12/01
REFERNCES AVAILABLE UPON REQUEST
Contact this candidate