Welcome to our online Fundamentals of Clinical Research training program! This comprehensive program is designed to equip you with the knowledge and skills necessary to excel in the field of clinical research. As a Clinical Research Associate/Monitor (CRA) or Clinical Research Coordinator (CRC) , you will play a vital role in the development and execution of clinical trials, ensuring the safety of participants and the accuracy of collected data.
Throughout this program, you will learn about various aspects of clinical research, including study design, protocol development, data management, regulatory compliance, and Good Clinical Practice (GCP) guidelines. Our curriculum is crafted by industry experts who have extensive experience in clinical research, ensuring that you receive the most relevant and up-to-date information.
Through a combination of modules followed by non graded MCQs, Scenarios, and practical exercises, you will gain a deep understanding of the responsibilities and best practices of a CRA and CRC. You will also explore real-world scenarios and challenges that you may encounter during your career. Our goal is to prepare you to confidently navigate the complex landscape of clinical research and make meaningful contributions to the advancement of medical knowledge.
Our online format provides you with the flexibility to learn at your own pace, allowing you to balance your training with other personal and professional commitments. You will have access to a dedicated support team who will be available to answer your questions and provide guidance throughout the program. Upon successful completion of the training, you will receive by mail an original certificate containing the seal of the Association, demonstrating your mastery of essential CRA and CRC skills and your readiness to embark on a rewarding career in clinical research. Just before completion of the course, we will provide you with guidance on career paths within clinical research, job search strategies, generic and job-specific questions and answers anticipated during interview and most importantly a guidance on ATS resume, cover letter that attracts recruiters/employers and LinkedIn Profile Optimization.
We are excited to accompany you on this educational journey and look forward to helping you achieve your professional goals as a CRA or CRC. Let’s get started!
- Blinding
- Clinical Trial Design
- Clinical Trial landscape (Players and Their Responsibilities)
- Clinical Trial Outcome/Endpoint
- Clinical Trial Phases
- Clinical Trials in The Context of Biomedical Research
- Controls of Clinical Trials
- Essential features (Objectives of clinical trials)
- Multi center Trials
- Randomisation
- Sample size
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