CLINICAL DATA MANAGEMENT AND SAS PROGRAMMING COURSES
Are you passionate about clinical data analysis and planning, clinical research, database design, SAS data analysis, reporting and data modeling, and want to be part of a clinical research team to support clinical trials? This career path is best for you. You must have a bachelor’s degree in science, statistics, mathematics, computer science, biotechnology, medicine, or healthcare administration to qualify. With Qtech-Sol Clinical data management training, we strive to achieve your career goals and make you a successful clinical data manager or SAS data analyst.
Clinical research is medical research that involves people. Clinical trials are research conducted on people to evaluate medical, surgical, or behavioral interventions. Researchers have discovered whether new therapies / new drugs, diets, or medical devices are safe and effective for people. Often, clinical trials are used to find out whether new therapies are more effective and/or have fewer harmful side effects than standard therapies. Clinical trials of drugs are often described in terms of their stage. (I, II, III and IV).
The Clinical Trial SAS Data Analysis and Reporting (CDAR) provides intensive learning on how SAS is used in clinical and pharmaceutical industries. In particular, how codes, analysis and reports are generated using SAS.
The Clinical Trial SAS Functional Programming (CDOT) provides learnings required to apply regulations, governance and procedures for analysis, monitoring and reporting clinical data using SAS Software.
SAS program is the industry-standard statistical tool. QPDC offers Basic SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various industries.
SAS program is the industry-standard statistical tool. QPDC offers Advanced SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various
Clinical Data Coordinators handle clinical information like patient records, appointments, studies, and other official documents. Their role is coordinating activities that relate to clinical administrative tasks and recording data for study and validation.
Clinical data managers are responsible for collecting data from a variety of medical research projects, such as clinical and pharmaceutical trials. They work collaboratively to make sure data is collected, managed, reported clearly, accurately and securely
THE ROLE OF SAS PROGRAMMER
SAS is widely used in clinical trial data analysis in pharmaceutical, biotech and clinical research companies. SAS programmers play an important role in clinical trial data analysis. In addition to doctors and clinicians who collect clinical trial data, the group conducting data analysis includes statisticians, clinical data managers (CDMs) and SAS programmers. Statisticians provide the ideas and methods of the data analysis; clinical data managers manage the collected data and control the data quality. In between, SAS programmers implement the analysis methods on the collected data and provide the study summary tables, data listing and graphs to the statisticians and for clinicians to write a study report.
|CDM Job titles qualified after this training|
|Clinical Data Manager||Clinical Data Research Specialist|
|Clinical Data Analyst||Case Report Form Designer|
|Data Quality Manager||Clinical Business Analyst|
|SAS Job titles qualified after training|
|Clinical SAS Programmer||SAS Data Analyst|
|SAS Data Modeling||Biostatistician|
|Program Manager||Clinical Data Scientist|