CLINICAL SAS FUNCTIONAL PROGRAMMING - Qtech-Sol USA offers Clinical Research / Trials, Pharmacovigilance, Drug Safety, Clinical Data Management, Clinical SAS Programming and Healthcare BA Training Programs
Category:
Data Management
 
Duration:
15 Weeks / 103 Days
 
 
 

Qtech-Sol Clinical SAS Functional Course

CLINICAL SAS FUNCTIONAL PROGRAMMING

Qtech-Sol is a Clinical Science Training Provider. This course provides lessons to learn on How SAS Program is used for Data Analysis and Reporting of Clinical Data across clinical trial phases. The program helps SAS programmers who wish to transition their career pathways for pharmaceutical jobs as Clinical SAS Programmer / Data Analyst. This is a job and title focused program. The course emphasizes about role and tasks performed by SAS Programmer to Analyze and Report clinical data captured from clinical trials or post marketing surveillance (Pharmacovigilance data). The course curriculum is designed to give an edge to obtain job as Clinical SAS Programmer / Analyst with Pharmaceuticals, Biotech, Medical Device, Clinical Research Organizations (CROs) and with Research Clinics

Course Name :  Clinical SAS Functional Programming
(Role based Lessons – Case Scenarios, Job Tasks with Solutions)
Code :  CDOT
Course Material : This course contains and delivers 35 Lessons.
Each Lesson contains various delivery modes as presentation with voice over, course reading material (chapters), Quizzes for Practice (15 Set) and Test (10 Set), Short Questions, Role based Tasks (Exercises, along with solutions).
Course Brochure : Download BROCHURE
Course Demo : Register for COURSE DEMO
Fill out Registration form and select module name Analytics and Reporting and select “Clinical Data Oriented Training” course. You will receive an email with weblink to self-activate your demo course. Upon activation will have access to 4 lessons for next 5 days.
Online Discussion : Book your slot for a personalized ONE-O-ONE discussion with us. You will receive an online invite to participate via email.
Application Form : APPLY NOW
To complete your enrollment, please email your resume to qpdc@qtech-solutions.com
Delivery Type

SIP – Self-Paced Online with Support

Course Duration

CDOT-SIP Delivery – 15 Weeks / 445 Hours / 103 Days (Self-Paced)

Introduction

SAS Software 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.

Course Enrollment process

Qtech-Sol offers self-paced online courses. Student get started with the course when they are ready. They must complete the online application, pay applicable tuition and submit required credentials. Student must submit their resume and copy of highest degree certificate obtained. These documents are used to validate the student’s name on certificate, contact information, course enrolled and their education eligibility to participate.

Start to Finish Steps:
  1. Submit Online Application
  2. Pay applicable tuition (Shopping cart)
  3. Email credentials required
  4. Receive Course Activation email
  5. Obtain access to Course and Solution bank (LMS)
  6. Receive support for subject related queries.
  7. Submit Course task deliveries per schedule shared
  8. Take Final exam upon completing he course
  9. Obtain Course completion certificate and transcript
  10. Get Started with PTA program for next steps
Gaining experience

An Ideal person must have bachelor’s degree in science or computer technology related disciplines to become a SAS Programmer. Qtech-Sol Clinical SAS Coursework is not wet lab experience, these are computer related roles performed using clinical data and tools, to support the progress of clinical trials being conducted. Person must have basic computer knowledge and few databases understanding, such as Oracle, SQL, Excel, Access etc. Works with Microsoft Word, Excel, Notepad, PowerPoint etc. The ideal person works within pharmaceutical or at hospital and research centers.

The Clinical SAS Programmer or SAS Data Analyst will develop and manage core area of clinical data obtained thru clinical trials or post marketing surveillance for data analysis and reporting needs. The person gets involved in SAS Efficiency Programming, Analysis and Validation of CRF data captured. Applies Good Clinical Practices, GxP regulations, Documentation using CRF Part 11 and SOP concepts, Performs Data Validation based on data types and protocol. participates to develop Statistical Analysis Planning and Hypothetical testing, Efficacy Data analysis using ISE and ISS concepts. Applies Clinical Data Interchange Standards Consortium (CDISC) concepts and creates datasets for reporting data as Tables Listing and Graphs (TLG). This program includes around 11 projects covering phase-wise clinical trial data towards Oncology, Ophthalmology, Cardiology and Central Nervous Systems (CNS) therapeutics areas. Also includes Pharmacovigilance and aggregate reporting concepts.

Examples of job titles to apply
  1. Clinical SAS Programmer
  2. Statistical Programmer
  3. Programmer Analyst
  4. Biostatistician
  5. Clinical Data Modeler
  6. Clinical Data Analyst
  7. Data Scientist
  8. SAS Data Analyst

  • Eligible Education:

    Recommended: A Bachelors or Master degree in Statistics, Biostatistics, Biotechnology, Economics, Computer Science, Engineering, Technology, Cognitive Science, Data Science or Mathematics.

    The Ideal person must know SAS Software Modules (Basics and Advanced). SAS software is required to successfully complete this “CDOT – Clinical SAS Functional Programming” course.

    Post Training Assistance

    Your resume is front face to hiring recruiters and organizations to pre-screen or call for an interview. With competition out in market, does your resume meet the requirements. Contact us to participate in our Post Training Assistance (PTA) program for resume build, interview narratives, and mock. It is as well important to know, the current hiring organizations in your area, open positions available, salary range, fitness of resume to apply and many more. During this PTA program you will have opportunity to discuss with our course specialist to learn and discover opportunities in small steps. We shall work together as team to achieve this goal.

  • Learning Outcomes:
    The Benefit Student Gains

    The Benefit Student Gains

    • Upgrading the Knowledge required.
    • Better Resume Placement for promising jobs.
    • Low Investment, high learnings
    • Learn from Anywhere, Anytime at your pace.
    • Job and Title Based Tasks as followed and Practiced in industry
    • Applying Concept into Real-time (Policies, governance and tools)
    • Work on Role Based Tasks followed and Practiced in industry
    • Mocks and Narratives for Client Discussions
    • Readiness to work with limited support
  • Professional organizations

    Professional organizations and associations are membership-based groups comprised of people working in a similar field. They can be helpful resources for students to learn more about a field, develop connections and discover related opportunities.

    Check out World-Wide Clinical Resource Information. Follow the resource links to learn what’s happening around the world on current news and updates about Clinical trials, Regulatory, CDM and Pharmacovigilance.

    Reviews

    Qtech-Sol has trained since 2000, many candidates with different education background and skills. Few of them are currently working as directors in top MNC companies.

    Thanks to Q tech for helping me to get back to workforce within 2 months. The CDOT program task-based exercises, provided me insight of role performed in real-time allowing me to get started at job right away.

    – Julee A – NYC

    This SAS CDOT training gave me a real-time job experience. The learning process was gradual, and the tasks were very interesting and very useful for gaining hands-on experience. I learned more when compared to my previous knowledge before starting this course. All the tasks and scenarios were different, and it was a very good learning experience.

    – Navya C – Dallas, Texas

    The Clinical Data Oriented SAS Program (CDOT) topics were very helpful to rate me. Chapters were organized better for easy readability. Very nice self paced SAS classes.

    – – Nisha D M K, Philadelphia, PA

    Getting Connected

    For additional information please call us on 732.770.4100 or ENQUIRE. One of our course specialists will contact you at earliest possible.

Curriculum Overview

Program is designed by industry experts meeting job and title-based learnings needed for students and young professionals to get into jobs. The training provides in depth knowledge of roles and responsibilities of Clinical SAS Programmer or Data Analyst. The curriculum includes theoretical and practical aspect of the role and tasks performed on day-to-day basis, along with exposure to various exercises per industry requirements.

Clinical SAS Functional Programming
Lessons Offered

1. Elementary SAS Concepts

2. SAS Efficiency Programming

3. Introduction to Clinical Trials

4. Types and Data in Clinical Trials

5. Clinical Trial Protocol Development

6. Elements of CRF Design

7. Electronic Data Capture (EDC)

8. Good Clinical Practices

9. Good Documentation Practices

10. Workflow Instruction Request

11. Documentation Templates

12. Introduction to Data Validation

13. Data-Based Validation

14. Protocol Based Validation

15. Basic of Statistics

16. Statistical Analysis Planning

17. Elements of Hypothesis Testing

18. Basic of Efficiency

19. Integrated Summary of Effectiveness (ISE)

20. Integrated Summary of Safety (ISS)

21. Clinical Data Interchange Standards Consortium

22. Preparing Analysis Data sets

23. Creating Tables Listing and Graphs (TLG)

24. Understanding Various Therapeutics Areas

25. Data-Based Therapy

26. Introduction to Phase I Studies

27. Oncology Project

28. Introduction to Phase II Studies

29. Ophthalmology Project

30. Introduction to Phase III Studies

31. Cardiology Project

32. Introduction to Phase IV Studies

33. Central Nervous Systems (CNS) Project

34. Introduction to Pharmacovigilance

35. Pharmacovigilance Reporting

Job focused exercises

1. Data-Based Validation

2. Protocol Based Validation

3. Elements of Hypothesis Testing (Pk, Pd and Dose)

4. Preparing Analysis Datasets and CDISC

5. Therapeutic – Oncology Project

6. Therapeutic – Ophthalmology Project

7. Therapeutic – Cardiology Project

8. Therapeutic – Central Nervous System (CNS) Project

9. Aggregate Reporting Process

10. SAS Efficiency Programming

11. Open CDISC Validator

Getting Connected

For additional information please call us on 732.770.4100 or ENQUIRE. One of our course specialists will contact you at earliest possible.

  • Thanks to Q tech for helping me to get back to workforce within 2 months. The CDAR program task-based exercises, provided me insight of role performed in real-time allowing me to get started at job right away.

    Julee A – NYC

  • This SAS CDAR training gave me a real-time job experience. The learning process was gradual, and the tasks were very interesting and very useful for gaining hands-on experience. I learned more when compared to my previous knowledge before starting this course. All the tasks and scenarios were different, and it was a very good learning experience.

    Navya C – Dallas, Texas

  • The Clinical Data Oriented SAS Program (CDAR) topics were very helpful to rate me. Chapters were organized better for easy readability. Very nice self paced SAS classes.

    Nisha D M K, Philadelphia, PA