Advanced SAS Clinical With CDISC Training
The purpose of Advanced SAS Clinical with CDISC Training is to give professionals the know-how to use SAS software to handle and analyze clinical trial data in accordance with CDISC (Clinical Data Interchange Standards Consortium) guidelines. This training focuses on advanced SAS programming techniques, data integration, and reporting to ensure that clinical data is managed effectively and complies with regulatory criteria.
- 10+ Courses
- 30+ Projects
- 400 Hours
Advanced SAS Clinical With CDISC Training is suitable for the following target audiences:
Clinical Data Managers: Experts in clinical trial data management who wish to improve their knowledge of SAS and CDISC standards.
SAS Programmers: Programmers working in the clinical research or pharmaceutical industries that want to focus on clinical trials and CDISC data submission regulations.
Biostatisticians: For more organized and compliant data handling, statisticians wishing to apply SAS programming and CDISC standards to their clinical trial analysis.
Clinical Research Professionals: People who work in clinical research and wish to expand their data analysis and reporting knowledge, such as Clinical Research Associates, or CRAs.
Regulatory Affairs Specialists: Regulatory affairs specialists ensure CDISC compliance by compiling and submitting clinical trial data to regulatory organizations.
SAS Clinical Programmer: Ensuring CDISC compliance while managing and analyzing data in clinical studies.
Clinical Data Manager: overseeing, verifying, and guaranteeing the caliber of clinical trial data in preparation for submission to regulatory bodies.
Biostatistician: A biostatistician applies statistical techniques to clinical data while following CDISC guidelines to ensure precise analysis.
Regulatory Data Submission Specialist: Complying with CDISC requirements while preparing and submitting clinical trial data to regulatory bodies (such as the FDA).
Clinical Research Analyst: Managing and evaluating clinical trial data for pharmaceutical corporations or CROs (Contract Research Organizations).
These positions, which offer good pay and chances for professional progression, are highly sought after in the USA and Canada, especially in pharmaceutical businesses, clinical research organizations, and healthcare facilities.
- Agile Overview
- Agile Manifesto & Principles
- Agile vs. Traditional (Waterfall) Approaches
- Scrum, Kanban, XP – overview of frameworks
- Role of a Business Analyst in Agile BA responsibilities in Agile teams
- Collaboration with Product Owner, Scrum Master, Dev Team
- Scrum Deep Dive
- Roles, Events, Artifacts
- Product Backlog, Sprint Planning, Review, and Retrospective
- Kanban Basics (WIP limits, continuous flow)
- Scaling Agile (SAFe, LeSS, Nexus) – intro level
- Tools included : Jira / Trello setup basics
- Gathering Requirements in Agile
- Just-in-time requirements
- Collaborative discovery
- User Stories & Acceptance Criteria
- INVEST criteria and Definition of Ready / Done
- Story Mapping & Backlog Grooming
- Jira / Confluence Training
- Backlog creation, story linking, boards
- Wireframing & Prototyping
- Tools: Balsamiq / Figma / Draw.io
- Facilitation Techniques
- Agile workshops (Story Mapping, Impact Mapping)
- Agile Planning Levels (Roadmap, Release, Sprint planning)
- Estimation Techniques (Planning Poker, T-Shirt sizing)
- Prioritization Methods (MoSCoW, Kano Model, WSJF)
- Performance Metrics (Velocity, Burnup/Burndown charts , Lead/Cycle Time)
- BA Contribution Metrics (Requirements churn, value tracking)
- How to create and maintain Dashboards in Jira
- Case Study: Analyse sprint reports & suggest improvements
- Stakeholder Management
- Effective Communication
- Facilitation & Conflict Resolution
- Agile Project Simulation End-to-end product backlog creation
- Resume Building for Agile BA
- Mock Interviews & Job Placement
This course is ideal for aspiring Business Analysts, working professionals transitioning to Agile roles, Product Owners, Project Managers, and anyone interested in Agile practices and business analysis.
No technical background is required. The course is designed to help non-technical individuals understand Agile concepts and tools in a practical, easy-to-follow manner.
The duration for Agile Business Analyst training is 2 months (8 weeks), with sessions held 2 times per week (either during week or weekends), including theory, hands-on practice and project work.
Yes, upon successful completion, you’ll receive a Certificate of Completion from Checkmate IT Tech. We also guide you on pursuing global certifications like IIBA-AAC and ICAgile-BA.
Absolutely! The course includes hands-on exercises, case studies, and a capstone project to simulate real Agile environments.
We offer online training classes to promote easy access to all candidates. Recordings are also made available for revision or if you miss a session.
Yes. We provide resume reviews, mock interviews, LinkedIn optimization, and guidance on job portals to help boost your chances in the job market.
You can enroll via our website or contact our support team directly via email or phone. We’ll guide you through the quick and easy registration process.
https://checkmateittech.com/
Email info@checkmateittech.com OR Call Us +1-347-4082054
- Submit Form
Job opportunities in USA and Canada
SAS Clinical Programmer: Ensuring CDISC compliance while managing and analyzing data in clinical studies.
Clinical Data Manager: overseeing, verifying, and guaranteeing the caliber of clinical trial data in preparation for submission to regulatory bodies.
Biostatistician: A biostatistician applies statistical techniques to clinical data while following CDISC guidelines to ensure precise analysis.
Regulatory Data Submission Specialist: Complying with CDISC requirements while preparing and submitting clinical trial data to regulatory bodies (such as the FDA).
Clinical Research Analyst: Managing and evaluating clinical trial data for pharmaceutical corporations or CROs (Contract Research Organizations).
These positions, which offer good pay and chances for professional progression, are highly sought after in the USA and Canada, especially in pharmaceutical businesses, clinical research organizations, and healthcare facilities.
