Programmer(SAS)

<h2>Job Overview:</h2><ul><li style="color: #000000;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">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</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">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</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">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</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Develop programs to import external data and transform to SAS Dataset or Excel files for data review and reconciliation</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Assist the Senior Programmers by performing report generations, Code review and reconciliation tasks, status update and other build, testing activities</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Maintain study databases for assigned projects and perform SAS programming as assigned by Managers. Prioritize workload to meet specified completion dates</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">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</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Ensure awareness of project-specific quality and performance standards and ensure that these are adequately documented, communicated and understood</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Contribute ideas to the development of the Department, identifying areas for improvement (e.g. SOPs, processes etc.)</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">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. </span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Continuously learn and improve communication, technical, good problem solving skills</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Perform other duties as assigned by Senior Programming staff</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="color: black; font-family: calibri, sans-serif; font-size: 10pt;">BE - Comp.Science, Information Technology, MCA with relevant Clinical SAS experience. Good to have SAS certification but not mandatory.</span></li><li style="color: #000000;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Good knowledge of drug development process and Clinical Data Management System Programming.</span></li><li style="color: #000000;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Good knowledge of relational databases</span></li><li style="color: #000000;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Fluent in English, both written and verbal</span></li></ul><h2>Experience:</h2><ul><li style="color: #000000;"><span style="font-family: Calibri, sans-serif; font-size: 10pt;">1 -3 years of relevant work experience to include data management and database support: SAS programming.</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: Calibri, sans-serif; font-size: 10pt;">Good problem solving skills and a proactive approach</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: Calibri, sans-serif; font-size: 10pt;">Good oral and written communication skills</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-family: Calibri, sans-serif; font-size: 10pt;">Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-size: 10pt;">Ability to work in a team environment and effectively under minimal supervision</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-size: 10pt;">Ability to prioritize work and Self-motivation</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-size: 10pt;">Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work</span></li><li style="color: #000000; font-family: 'Calibri',sans-serif; font-size: 11pt;"><span style="font-size: 10pt;">A cooperative and team-oriented approach</span></li></ul>