x

Whatsapp Enquiry

Hello Welcome to HCI Whatsapp Chat Introduce yourself

Advanced Post Graduate Diploma in Clinical Research, Biostatistics & SAS

Advanced Post Graduate Diploma in Pharmacovigilance

Program Structure

This is a comprehensive educational program, designed for the Pharma /Medical/Life Sciences professional aspiring to work in the field of clinical research or allied professions like central labs, CROs, Sponsor Company

  • The program provides complete overview and practical environment in the field of clinical research
  • The program would help candidates to upgrade their knowledge about ICH GCP Guidelines, regulatory issues, study design, research methodology, and statistical analysis and interpretation in clinical trials and other major aspects of clinical trials management.
  • Course has been divided into four modules
  • In First module, we cover the basic aspects of Clinical research design, planning and management
  • The second module would include Biostatistics which help the learner to understand the subject thoroughly
  • In the third module, we are focusing on SAS programming
  • In the fourth module, we cover clinical data analysis and reporting using SAS software
  • Program would help in developing career in the field of clinical research.

Advantages of the Program

  • Industry Accredited / Certified
  • Application of Clinical Research & Pharmacovigilance in real business-like environment.
  • Completely Job Oriented – Hands-on Training
  • Accredited by Accreditation Council for Clinical Research Education, USA (ACCRE) & Certified by Pharmaceutical Society of India.
  • 100% placement Support– Excellent Placement Record
  • Training by the team of industry experts – both full time and visiting senior faculty.
  • Small Batch – 15 seats

Back to Courses

Clinical Research

Basics Of Clinical Research
  • Clinical Research Introduction
  • Principles of Pharmacology & Drug Discovery & Development
  • Roles & Responsibilities of Key Stakeholders
  • Preparations & Planning for Clinical Trials
  • Essential Documentation in Clinical Research & Regulatory Submissions
  • Clinical Trials Project Planning & Management
  • Study Start Up Process
  • Clinical Monitoring Essentials
  • Compliance, Auditing & Quality Control in Clinical Research
  • Clinical Data Management, Biostatistics, Analysis & Reporting
Basics Of Biostatistics
  • Introduction to Research and Statistics/Descriptive Statistics/Probability
  • Distributions
  • Sampling Distributions/Statistical Inference
  • Correlation and Regression
  • Choosing Statistical Tests/ T-Test, Chi-Square Test, ANOVA, etc
  • Analysis of Categorical Data and Non Parametric Tests
  • Introduction to Statistical Software’s
Sas Programming
  • Getting Started with SAS
  • Components of SAS
  • Reading various types of Raw data
  • Working with SAS Datasets
  • Combining datasets
  • Working with SAS Arrays
  • Proc SQL
  • SAS Macro Language
  • Basic Statistical Procedures
Clinical Data Analysis And Reporting Using Sas Software
  • Introduction to Clinical Trials
  • Understanding and Reviewing Statistical Analysis Plan
  • Annotating the Mock Tables
  • Creating Dataset Specifications
  • Creating Analysis Datasets
  • Creating Tables/Listings/Figures

Study Methodology

Hands on training on software, online live classes/distance learning

Examination

Online MCQs/Classroom

Certificate

Post Graduate Diploma would be awarded upon successful completion of the program. Program accredited by Accreditation Council for Clinical Research Education, USA.

Faculty

Training would be imparted by the fulltime Think I & Cliniminds faculty and visiting experts from the industry.

Validity

Life Long

Class Mode

E learning {6 Months without internship)
Distance Learning {6 months}

Please contact counsellor for upcoming batch details 91 812 910 0876 / 91 484 421 6666 / 1800 1023 566 (Toll Free)

PAY ONLINE

COURSE FEE
Actual Fee 99000+18% GST

*Inclusive of applicable tax

INR 116820.00 *

Quick
Enquiry