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Db Developer Resume

Exton, PennsylvaniA

Over 20+ years of industry experience:

  • Anti-Infective, Diabetic, Gastrointestinal, Neuropathy, Respiratory, Oncology, Ophthalmology, Orthopedic and Urology Phase I, II, III and IV experience
  • Proficient in Oracle Clinical
  • Extensive experience designing Case Report Forms
  • 10 years of experience programming and writing edit checks

EDUCATION: Confidential

PROFESSIONAL EXPERIENCE:

Confidential, Exton, Pennsylvania. May 2010 to Present

Position: Contractor DB Developer

  • Create Data Entry Screen in Oracle Clinical from CRFs
  • Test Data Entry Screens in Oracle Clinical
  • Program edit checks
  • Design CRFs
  • Create listings and datasets in SAS
  • CDM manager of clinical studies
  • Reviews CRFs and issues queries

Confidential,Malvern, Pennsylvania. Database Designer, September 2007 to 2010
Position: Database Designer - GV

  • Create Questions and Question Groups within Oracle Clinical
  • Create character and graphic layouts for screens in Oracle Clinical
  • Maintain Global Library standards in CDISC format within Oracle Clinical
  • Test Data Entry Screens in Oracle Clinical
  • Program and maintain standard and study edit checks
  • Standard team member whom collaborates between CDM and Biostats depts.
  • Create and/or validate changes that apply to the global standard modules as deemed necessary
  • Supply documentation for validation and testing
  • Aided in applying, testing, validating and training a Lab maintenance system package
  • Aided in applying, testing and validating a TMS system package
  • Supports and lends guidance to the study DB developers
  • Writes internal documentation for guidelines and SOPs

Confidential, Exton, Pennsylvania. December 2001 to August 2007
Has Held the following positions:
DB Developer II, 2007
DB Developer I, 2003 to 2007
CDM Associate, 2001 to 2003

  • Create Data Entry Screen in Oracle Clinical from CRFs
  • Test Data Entry Screens in Oracle Clinical
  • Programmed edit checks and derivations
  • Maintain Global Library
  • Laboratory data reconciliation
  • Writing of internal documentation and SOPs
  • Design and annotate CRFs
  • Create listings and datasets in SAS
  • CDM manager of clinical studies
  • Training of staff in Oracle Clinical
  • Validated system during upgrade

Confidential, King of Prussia, Pennsylvania. November 1993 to November 2001 Held the following positions:
Database Coordinator II, February 2001 to November 2001
Database Coordinator, October 1999 to February 2001

  • Created Data Entry screens in Oracle Clinical from CRF\'s
  • Tested DE screens in Oracle Clinical
  • Created Derivation Procedures
  • Wrote internal Documentation
  • Responsible for coordination of information between TMS and Oracle Clinical
  • Trained staff in Oracle Clinical
  • Global Librarian for Oracle Clinical
  • Assisted the Programmers and Edit Developers in development of protocols
  • Assisted with filing CRFs and maintaining order in file rooms
  • Alerted CDA\'s and Managers to any potential problems discovered in the DE/DDE process
  • Assisted CDA\'s with maintaining project specific documentation binders
  • Ran edit reports and case listing reports

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