Db Developer Resume
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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