Job Overview:
•Read, understand and program EDC objects/SAS programming as per the specification documents which meets client requirements and projects.
•Work on EDC edit checks, DB design, custom functions, SAS checks, listings as required with guidance from senior staff.
•Complete assigned work utilizing Medidata RAVE or Oracle InForm or SAS or other proprietary software according to Covance SOPs, Work Instructions ,and project specific guidelines in accordance with Good Clinical Practices
•Prioritize personal workload to meet specified completion dates.
•Maintain and program study databases for assigned projects and SAS programming as assigned by managers.
•Perform all work with knowledge of regulations pertaining to computerized systems to projects to ensure compliance.
•Ensure quality of personal work
•Interact with project team members in related discipline e. g. Clinical Data Management, Clinical Operations and Data Management.
•Display a positive attitude at all times, promoting and contributing to good team spirit in a professional environment
•Continuously learn and improve communication and technical skills.
•Attention to detail is essential and all tasks must be carried out to the highest standard.
•Develop good problem solving skills and a willingness to learn and seek advice from senior Programming staff
•Acquire knowledge of other aspects of the work of a Associate Programmer under the supervision of the senior Programming staff
•Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
•Perform other duties as assigned by senior Programming staff
Education/Qualifications:
• BCA/MCA/BSc Computer Sciencce/MSc Computer science
•Basic knowledge of Drug Development process and Clinical Data Management System Programming.
•C# .Net programming knowledge is preferred