JOB SUMMARY:
Responsible for ensuring the validity of clinical trial data. Format and organize data for medical review and statistical analysis. Assist in implementing study specific procedures compliant with Regulatory and internal procedures and requirements. Execute data management plans for the implementation and management of data collection, review, clarification and reporting systems for clinical studies. Create database design and edit check specifications through spreadsheets and determine data field name and properties. Validate database design in a test environment to test all aspects of the database design. Reviews automated validation system output and determines appropriate course of action to resolve data discrepancies according to established Standard Operating Procedures (SOPs).

BACKGROUND REQUIRED:
Knowledge of Good Clinical Practice requirements
Strong project management skills
Organizational, verbal and interpersonal skills

DESIRED:
Associates degree in a science field
Familiarity with major data management functions
Knowledge of database architecture and structure
Knowledge of and experience with data processing, quality control and audit procedures
Programming experience (PL-SQL or SAS)

Email WORD resume to: Plymouth@entegee.com. Refer to job #12117281pw.