SAS ( Statistical Analysis Software) is a pivotal part of whole clinical research process provides the analysis to the data captured from the patients into the clinical trails before the submission to US FDA or any regulatory body to all the pharmaceutical and clinical research industry by accessing
SAS ( Statistical Analysis Software) is a pivotal part of whole clinical research process provides the analysis to the data captured from the patients into the clinical trails before the submission to US FDA or any regulatory body to all the pharmaceutical and clinical research industry by accessing, analysing and reporting clinical data in an accurate way.
As a Clinical/ Statistical /SAS programmers implement the analysis methods on the collected data and provide the study summary tables, data listing and graphs to the statisticians, medical writers and clinicians to use in writing the clinical study report. Clinical programmers work closely with clinicians, biostatisticians and data managers and provide an important interface that helps provide the linkage between CRF data and the intended analysis.
While data is being re-entered and cleaned, statistical clinical programmers may begin to write SAS programs to generate report tables, listings, and graphs according to the statistical analysis plan (SAP) and the tables shells designed by the study biostatistician. Drafts of tables, listings and graphs· are reviewed by the statisticians and more data clarification items may also be generated in this process.
Since a programmer often needs to interact with different functions, the work becomes more meaningful if they have a brief understanding of the roles performed by each of the study team members from the CTM, PV, MW, SAS and RA departments.
Xcelcareer – Since our inception over 2 decades we have been in the forefront in clinical research training certification and assured placement for our students in Pharma and healthcare sectors including sought after IT Healthcare careers such as Pharmacovigilance, Clinical SAS and Clinical Data Management.
Our prime focus is to uplift Pharmacy, Lifesciences, and Medicine including Paramedical graduates into Clinical Research Industry with our unmatched long time Industry networks and tie-ups to provide deserving jobs and a smile to an aspirant.
We also take immense pride in saying that we have a wonderful team of hand-picked industry-relevant trainers who come with a rich knowledge of current trends and scenarios which in turn becomes a boon to our students to get hands-on knowledge for their future job opportunities and career of their own interest.
Our Flagship program is a combination of Industry Skill Enhanced Professional certificate ( ISEPC ), P.G Diploma programs in Clinical Research (Clinical Trial Management), Pharmacovigilance, Medical Writing, Scientific Writing, Clinical Data Management, Clinical SAS, Regulatory affairs, Pharma & Health Business Management Training. In fact, we also modify it based on the industry standards keeping in mind the recent scenario and the job market for our students.
Certification Course in Clinical Research Training is offered by KCRI (Karnataka Clinical Research Institute). KCRI Bangalore, provides the best Training for Clinical Research courses, we are providing online/offline both training modes.
Clinical Research course is offered by Apollo Research and Innovations (ARI). To fulfil the demand and supply gap for skilled and trained clinical research professional in the pharmaceutical and biotechnology industry Apollo Research and Innovations (ARI)
This Clinical Research course trains students on domain knowledge of clinical research/trial and prepares them for jobs in clinical research in just three months through our training and support.
The Clinical Research Fundamentals course helps people who want to become professionals by teaching them all about clinical research basics. This includes learning about how research is done, the rules to follow, and how to be fair.
Clinical Research is the backbone of medical advancements. In the APCRM course, you’ll learn the fundamentals of clinical trials, regulations, and ethical considerations.
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