Diploma in Clinical Research

60 hours – 6 months

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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. During a trial, detailed information is gained about a new treatment, its risk and how well it may or may not work.

Diploma in Clinical Research is designed to provide candidates with an opportunity to acquire and develop the expertise necessary for effective clinical research. The program is designed to meet the high demand for trained personnel for human clinical trials.

600/- GBP including tuition fee, Examination etc

At the end of the program, successful candidates will receive Diploma in Clinical Research from ICRI Global Research and they will be eligible to apply for Higher Diploma and Degree level programs.

The programme utilises net-based delivery with online lectures, assignments. Additionally, optional classroom interaction sessions are conducted over a weekend at ICRI Global Research campus in U.K.

Minimum 18 years of age and high school completion or its equivalent with lifesciences background. Students need competency in, or completion of a basic computer operations course. Student will be required to have access to the internet, printing capabilities and an email address.

Students will be intimated if any suitable job requirements come up at ICRI Global Research Career Center. Typically starting salaries Rs. 12,000/- to Rs. 40,000/- per month.

• Candidates wanting to pursue a career in the field of clinical research.
• Individuals who have 6 to 12 months Clinical Research experience.
• Candidates who are looking at an industry shift to clinical Research.

• Clinical Research associate
• Project Manager
• Drug safety officer
• Pharmacovigilance Manager
• Clinical data manager
• Regulatory Affairs personnel
• Business Development
• Medical writing
• Medical investigator
• Co-investigator and many more…

• Learn the process of drug development
• Gain an understanding of the clinical trials process through a operations-focus approach
• Acquire overview of Pharmacology & Biostatistics
• Gain a global perspective on clinical trials management to better respond to the growing industry across the globe
• Learn about the ethical issues inherent in clinical trials
• Know the statistical methods to monitor clinical trial outcomes and make decisions
• Gain practical knowledge through real-world case studies and team projects in product development
• Learn about Quality control and Auditing of Clinical trials
• Introduction to Pharmacovigilance and safety reporting

• Presentations
• Individual study
• Classroom interactions
• Group Discussions
• Independent Research

• Quizzes and Assignments
• Written test
• Independent project work
• Group Discussions
• Independent Research