Indian Institute of clinical Research & Management (IICRM)offers the following courses looking at current demand in the market.
COURSES AT IICRM
PG diploma in clinical research & management (one year).
PG diploma in clinical research & management (part time/ 6 month).
Online training & Diploma courses
PG diploma in Clinical Data Management.
PG diploma in Pharmacovigilance.
M.Sc in Clinical Research 2 year.
Clinical SAS
These programs are designed for the professional who wants to transition into a Clinical Research Associate/ Clinical Research Investigator/ Study Coordinator/ Data Manager/ Biostatistician/ Regulatory Affairs Managers/ Clinical Trials Auditor/Clinical Project Manager/Clinical Research Manager/ Business Development Manager/ Drug Safety Associate/Medical Writer or enter the clinical research industry. It offers a comprehensive Education and “Hands-On” Training of the clinical research process, the FDA regulations, GCP (Good Clinical Practice) and the International Conference of Harmonization (ICH) guidelines. Over 15000 people have successfully completed our program
Indian Institute of clinical research & Management has expanded to provide individuals with additional training options via class room / distance learning system providing flexible and affordable clinical research training via comprehensive training programs, education modules and interactive Webinars.
On-site services for institutions in need of clinical research training
Job Prospects
Over the year 25,00000 jobs are available in this field
Course Description:
PG diploma in clinical research & Management,
an interactive program providing distance and classroom training for the clinical research professional, begins with the history of legislation and regulations that govern clinical research and an overview of drug, biologic, and device development. Course participants develop a thorough knowledge base of Good Clinical Practices and International Conference of Harmonization guidelines (E6, E2A), gaining a solid understanding of clinical trial development and management.
The Part 2 classroom
training focuses on developing a systematic approach to monitoring, conflict resolution, and problem solving. The participants monitor 6 study subjects and 3 regulatory binders across two study types. Writing effective and professional monitoring reports is also addressed. During the review and discussion of GCP issues, the instructor highlights the differences between device and drug/biologic studies
This course is designed to provide a brief overview of clinical research, terminology, and acronyms followed by a comprehensive review of FDA GCP and ICH GCP (E6). It also reviews the fundamental elements involved in coordinating a clinical trial from the investigator’s perspective. It includes practical tips and suggestions that can be applied to promote a GCP and HIPAA compliant clinical trial, including preventative measures and problem solving techniques of some of the most common GCP non-compliance issues.