About Us:

PRIVATE CAREER SCHOOL

(Approved by NJ Dept. of Education and Dept of Labor & Workforce Development)

Qtech-Sol Professional Development Center (QPDC) certificate programs are backed and approved by New Jersey Department of Education (DOE) and the Department of Labor and Workforce Development (DOL). We primarily focus on Clinical Research and Trials, Drug Safety-Pharmacovigilance, SAS Data Analytics, and Reporting, Clinical Research Data Management, Clinical Research project Management and Healthcare Business Analysis.

 

Details:

Qtech-Sol is looking for aspirant students interested and looking to gain experience as practicum needed for Clinical Science Careers. This Clinical Trial SAS Data Analysis and Reporting (CDAR) program is offered for first 10 selective students subject to interview performance, GPA and meeting eligibility requirements. This is domain-based unpaid practicum, allowing student to gain the experience needed. The learning is tailored per job title and duties as assigned by industry. Practicum learnings of the job is delivered with mix of presentation, quizzes, short description questions and various job specific exercises, along with solutions. At the end the student is subject to take a final exam for certification and recommendations. The learning gained allows the student to apply for various job titles as listed below. Get hands-on required to perform as Clinical SAS / Statistical Programmer with various Pharmaceuticals, Research Hospitals and Clinical Research Organizations (CROs) as Drug Safety-Pharmacovigilance Data Management specialist.

Role of Clinical SAS Data Analyst

Statistical programmers are a variety of statistician who specialize in creating computer software that can collect, analyze and report information from large databases. Statistical programmers can find work in a number of fields, from biotech and pharmaceutical research to the court systems to corporate offices. Write SAS programs to generate tables, listings, and figures and analysis datasets. Review CRF annotations and data specifications. Works with Biostatistics and Data Management members on various clinical projects. Identify and edit checks per the data validation plan or data management plan.

Post Training Support (PTA)

Upon evaluation of submitted tasks a course completion certificate, recommendations and student performance report is shared. Post Training Assistance program is offered for job readiness and this program includes resume preparation, narratives mock session and referral as Intern.

Program Details

https://qtech-solutions.com/program/clinical-trial-sas-data-analysis-reporting-cdar

Students who do not know SAS Software, will first get trained in SAS, prior to starting this CDAR program.

• SAS Basic Modules (BSAS) – Base, Macros and Sql
• SAS Advanced Modules (SSAS) – Stat and Graphs

 

Who is Eligible / Education:

Junior and Senior students pursuing,
Bachelor or Master or PhD in Statistics, Biostatistics, Mathematics, Computer Science, IT, Data Analytics

SAS Software

Student must have SAS 9.X Software installed in their PC, to participate in this CDAR Program.