Clinical Research Certification Training Program
Duration: 2.5 Months
Clinical Research
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, more and more
information is gained about a new treatment, its risks and how well it may not work.
Program Summary
Certification in clinical research (CCR) 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.
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.
Course Fee
Rs. 24,000/- +GST including study material.
Eligibility
Minimum 18 years of age and high school completion or its equivalent with
life sciences 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 email address.
Program Outline
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
Program Objectives
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
To Prepare For Jobs As
Clinical Research Coordinator
Clinical Research Associates
Clinical Research Assistants
Patient Recruitment Executive & more