Job Openings >> Contract Clinical Database Programmer 2
Contract Clinical Database Programmer 2
Summary
Title:Contract Clinical Database Programmer 2
ID:335847
Department:Development
Description

Position : Contract Clinical Database Programmer 2

Location : Franklin Lakes, NJ

Duration : 5 Months

Total Hours/week : 40.00

Client: Medical Device Company

Job Category: Technical

Level Of Experience: Senior Level

Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)

 

Job Description:

  • The Clinical Database Programmer will lead the development and maintenance of database builds in support of clinical studies.
  • He / she will build study databases including development of database specifications/definitions, programming of CRF layouts, programming of validation and derivation procedures, and programming of various reports to support the data review process.
  • The Clinical Database Programmer will troubleshoot technical issues as required for staff regarding specific database issues.
  • He / She contributes to the continual process development within the data management group and helps define best practices.

 

Essential Job Functions:

  • Develops database design specifications/definitions in consultation with data management, statistics and programming.
  • Designs and creates clinical databases to enable data review/validation of the study data by Data Managers, and a comprehensive and efficient analysis by Statistics and SAS Programming.
  • Programs and tests database configurations (edit checks, derivations, form/field dynamics, etc.).
  • Programs and tests reports using SQL/SAS to identify inconsistencies and support data review efforts.
  • Performs pre-processing and loading of non-CRF data files.
  • Contributes to solutions for routine technical problems and liaises with IT as appropriate to resolve issues.
  • Identify and implement solutions to data management issues and concerns that arise during the conduct of the study.
  • Identifies and understands the need for standardization and takes initiative to help improve departmental efficiency.
  • Establishes and maintains productive working relationships with all other functional areas that contribute to the execution of clinical studies.
  • Contributes to the development of Departmental SOPs, Business Guidance and/or Standards/Templates to define best practice and promote consistency.
  • Maintains all required study documentation.

 

Required Qualifications:

  • Proficient in Oracle SQL programming
  • Understanding of relational databases.
  • Experience with development, validation, execution, maintenance, documentation, and archival of clinical data targeted for regulatory submission.
  • Ability to work independently with minimal supervision and manage multiple deliverables concurrently.
  • Ability to ensure clinical database programming work is completed in a consistent manner and validated according to department practices.
  • Excellent interpersonal skills, strong written and verbal communication skills.
  • Working knowledge of clinical development.
  • Working understanding of clinical trial principles and technical implications.
  • Ability to interact effectively within and across team environment.
  • Ability to travel up to 10% of the time

 

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