Certificate in Clinical Research for Investigators

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Clinical Research refers to a study conducted to evaluate a potential treatment and its effects on human beings. Clinical trials help us find out if a promising new treatment is safe and effective.

Clinical Research market provides global opportunities at a huge size. In Asia alone, the Clinical Research market is worth more than US$2.5 billion. There is a high demand for trained investigators who get paid large amounts to conduct clinical trials independently.

Certification in Clinical Research for investigators (CCRI) is designed to provide candidates with an opportunity to acquire and develop the expertise necessary to take up roles of an investigators/ Co-investigators or Clinical Research Associate

The program enable you to master practical aspects of clinical trial conduct and management including clinical trial phases and design, planning, implementation, data analysis, regulatory and procedural guidelines and ethical considerations.

investigators are the senior most people at a Clinical Trial site. As an investigator/ Co-investigator, you not only supplement your income but also add to your knowledge and help discover new medicines.

600/- GBP

At the end of the program, successful candidates will receive Certificate in Clinical Research from ICRI Global Research, UK which is a globally recognized qualification.

The programme utilises Net-based delivery with online lectures, assignments. Additionally, classroom interaction sessions are conducted across all campus in Asia,U.K. and U.S.A.

Minimum qualifications are MBBS, MD or DM Candidates need to have access to the internet, printing capabilities and an email address.

20000 GBP to 100000 GBP

A database will be created of all the successful candidates which will be made available to all potential recruiters such as CROs/ Pharma companies etc.

• Introduction to Clinical Research.
• Basic Pharmacology & Pharmacy in CR
• New Drug Development
• Guidelines For Clinical Trials (ICH - GCP)
• Ethics in Clinical Research
• Regulations in Clinical Research
• Biostats & Clinical Trial Designs
• Clinical Trial Documents
• Quality in Clinical Trials
• Clinical Trial Management -Project Management
• Drug Safety & Pharmacovigilance
• Clinical Data Management

• Learn the process of drug development
• Gain an understanding of the clinical trials process though a operations-focus approach
• Acquire overview of Pharmacology & Biostatistics
• Gain a global perspective on clinical trials management to better respond to the growing industry
• Learn how to respond to ethical issues inherent in clinical trials
• Gain practical knowledge through real-world case studies discussions
• Learn about Quality control/ Auditing of Clinical Trials
• Appreciate the process of pharmacovigilance and Safety reporting

• Clinical Research Principal investigator
• Clinical Research Co- investigator
• Clinical Research Associate

• Multimedia Presentations
• Online sessions
• Classroom interactions
• Group Discussions
• Independent Research

• Quick Quizzes
• 4 Assignments
• Case study / Discussions
• 2 Written test
• Viva voce