Clinical Research Training
Clinical Research Training Online by Checkmate IT Tech offers a transformative journey, elevating your expertise and mastering essential skills. Position yourself for success in the dynamic field of Healthcare Technologies by enrolling today. Unlock new career opportunities!
- 10+ Courses
- 30+ Projects
- 400 Hours
Healthcare Professionals: Physicians, nurses, and other healthcare professionals who want to advance their knowledge of clinical trial management or move into clinical research positions.
Graduates in the life sciences: People who want to work in clinical research yet have degrees in biology, biochemistry, pharmacy, or similar disciplines.
Clinical Trial Coordinators and Monitors: Clinical trial coordinators and monitors are experts who now oversee or manage clinical trials and who wish to develop their abilities and further their careers.
Professionals in regulatory affairs: Those working in regulatory compliance who want to learn more about the rules and procedures of clinical trials.
Pharmaceutical and Biotechnology Employees: Workers in the pharmaceutical and biotechnology sectors: Workers in these sectors who wish to improve their understanding of clinical trials and research techniques.
Clinical Research Coordinator (CRC): A clinical research coordinator (CRC) is in charge of managing the daily operations of clinical trials, including data collecting, patient recruiting, and regulatory compliance.
Clinical Research Associate (CRA): A clinical research associate (CRA) monitors clinical trial locations to ensure rules, procedures, and data correctness are followed.
Regulatory Affairs Specialist: Ensuring clinical trials adhere to ethical norms and local, national, and worldwide legislation.
Clinical Data Manager: Overseeing and evaluating data gathered during clinical trials to guarantee precision and dependability.
Clinical Trial Manager: Overseeing and directing clinical trial teams to ensure efficient and timely study execution.
Pharmacovigilance Specialist: Ensuring drug safety by tracking and reporting adverse occurrences or side effects from clinical studies.
Biostatistician: A biostatistician examines trial data and offers statistical analysis to inform choices.
Contract research organizations (CROs), government health agencies, academic research institutions, biotechnology, and pharmaceuticals provide many opportunities. These positions, which offer good pay and opportunities for professional progression in the USA and Canada, are in high demand because of the increased focus on clinical trials for new medication development.
- 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
Clinical Research Coordinator (CRC): A clinical research coordinator (CRC) is in charge of managing the daily operations of clinical trials, including data collecting, patient recruiting, and regulatory compliance.
Clinical Research Associate (CRA): A clinical research associate (CRA) monitors clinical trial locations to ensure rules, procedures, and data correctness are followed.
Regulatory Affairs Specialist: Ensuring clinical trials adhere to ethical norms and local, national, and worldwide legislation.
Clinical Data Manager: Overseeing and evaluating data gathered during clinical trials to guarantee precision and dependability.
Clinical Trial Manager: Overseeing and directing clinical trial teams to ensure efficient and timely study execution.
Pharmacovigilance Specialist: Ensuring drug safety by tracking and reporting adverse occurrences or side effects from clinical studies.
Biostatistician: A biostatistician examines trial data and offers statistical analysis to inform choices.
Contract research organizations (CROs), government health agencies, academic research institutions, biotechnology, and pharmaceuticals provide many opportunities. These positions, which offer good pay and opportunities for professional progression in the USA and Canada, are in high demand because of the increased focus on clinical trials for new medication development.
