Who you are: Advanced degree in Life Sciences (e.g. Additionally, you will be accountable for establishing and maintaining effective program and study level communications with the respective Program, Trial Data Managers, and other key data stewards. Furthermore, you will support the assessment of the Data Standards Quality of clinical study including datasets, documentation (cSDRG) and define.xml. You will leverage those tools for applicable studies to ensure key risk indicators (KRIs) for clinical data, and key quality indicators (KQIs) for operational data are properly defined. As a Senior Data Quality Specialist, you will be working closely together with our Program and Trial Data Managers, and other data stewards to drive value creation by assessing the completeness, quality, and integrity of clinical and operational data by using advanced tools. Your role: an exciting opportunity has arisen to join our healthcare business to support the development of first and best in class specialty medicines for our patients in need. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. For more than 350 years and across the woĪ career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. Expertise in Custom Function knowledge is preferredExperience:2-5 years of experience in edit check programming, migrations and custom functions.A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics.Basic knowledge of Drug Development process and Clinical Data Management System Programming.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).Perform other duties as assigned by Manager.Education/Qualifications:MCA, BCA, MSc CS, BSc CS, B-Pharma.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).Acquire knowledge of other aspects of the work of Programmer/Analyst under the supervision of the senior Programming staff.Develop good problem solving skills and a willingness to learn and seek advice from senior Programming staff.Attention to detail is essential and all tasks must be carried out to the highest standard.Continuously learn and improve communication and technical skills.Display a positive attitude at all times, promoting and contributing to good team spirit in a professional environment.Clinical Data Management, Clinical Operations and Data Management. Interact with project team members in related discipline e.Perform all work with knowledge of regulations pertaining to computerized systems to projects to ensure compliance.Maintain study databases for assigned projects and SAS programming as assigned by managers.Prioritize personal workload to meet specified completion dates and perform work with supervision and direction from managers. Perform quality check and ensure the work is delivered with 100% quality.Mentor the team to make them independent enough to perform day to day activities.Train the team on Rave or SAS as required and have them ready to perform the regular day to day activities.Provide suggestions and solutions to the operational issues. 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.Perform publish checks, complex structure dynamics, RSG, Balance mapping settings.
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