Programmer(SAS)
Laboratory Corporation of America Holdings (Covance)
Bangalore, India
3d ago
  • Proactively learn to design and execute processes related to programming, setup, support of clinical and / or safety databases like Medidata Rave or Oracle InForm or SAS programming
  • Perform the following duties with minimal guidance from senior staff Database design, EDC / SAS edit programming, listings, ad-hoc / scheduled reports using SAS / Cognos / Business Objects - XI / R and other tools for data clearing and reporting
  • Complete assigned work utilizing EDC tools or SAS or other proprietary software according to Labcorp Drug Development SOPs, Work Instructions, project guidelines in accordance with Good Clinical Practices
  • Develop programs to import external data and transform to SAS Dataset or Excel files for data review and reconciliation
  • Assist the Senior Programmers by performing report generations, Code review and reconciliation tasks, status update and other build, testing activities
  • Maintain study databases for assigned projects and perform SAS programming as assigned by Managers. Prioritize workload to meet specified completion dates
  • Perform all work with knowledge of regulations pertaining to computerized systems to projects to ensure compliance and interact with project team members in related discipline
  • Ensure awareness of project-specific quality and performance standards and ensure that these are adequately documented, communicated and understood
  • Contribute ideas to the development of the Department, identifying areas for improvement (e.g. SOPs, processes etc.)
  • Train and mentor the team on EDC tools or SAS as required and have them ready to perform independent enough on day to day activities.
  • Continuously learn and improve communication, technical, good problem solving skills
  • Perform other duties as assigned by Senior Programming staff
  • BE - Comp.Science, Information Technology, MCA with relevant Clinical SAS experience. Good to have SAS certification but not mandatory.
  • Good knowledge of drug development process and Clinical Data Management System Programming.
  • Good knowledge of relational databases
  • Fluent in English, both written and verbal
  • 1 -3 years of relevant work experience to include data management and database support : SAS programming.
  • Good problem solving skills and a proactive approach
  • Good oral and written communication skills
  • Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred
  • Ability to work in a team environment and effectively under minimal supervision
  • Ability to prioritize work and Self-motivation
  • Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work
  • A cooperative and team-oriented approach
  • 2021-10-08 10 : 09 : 31

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