•Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE, Oracle InForm and SAS programming.
•Read, understand and program EDC objects/SAS programming as per the specification documents which meets client requirements and projects.
•Perform any post production changes to the EDC data base or enhancements to the SAS programs like SAS edit checks, listings, Reconciliation listings, Protocol Deviations, ACDR listings etc.
•Perform publish checks, complex structure dynamics, RSG, Balance mapping settings.
•Complete assigned work utilizing Medidata RAVE or Oracle InForm or SAS or other proprietary software according to Labcorp Drug Development SOPs, Work Instructions ,and project specific guidelines in accordance with Good Clinical Practices
•Provide suggestions and solutions to the operational issues.
•Train the team on Rave or SAS as required and have them ready to perform the regular day to day activities.
•Mentor the team to make them independent enough to perform day to day activities.
•Perform quality check and ensure the work is delivered with 100% quality.
•Prioritize personal workload to meet specified completion dates and perform work with supervision and direction from managers.
•Maintain 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 Programmer/Analyst under the supervision of the senior Programming staff
•Carry out all activities according to Labcorp Drug Development SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
•Perform other duties as assigned by Manager.
MCA, BCA, MSc CS, BSc CS, B-Pharma
•University/college degree (Life Science, Computer Science, Programming, Pharmacy or related subject preferred), or certification in a related profession from an appropriately accredited institution (e.g., Nursing Certification, Computer Science, Medical or Laboratory Technology)
•Basic knowledge of Drug Development process and Clinical Data Management System Programming.
•Expertise in Custom Function knowledge is preferred
2-5 years of experience in edit check programming, migrations and custom functions.
Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed