PG Diploma in Clinical Research
ONLINE | CLASSROOM | CAMPUS TRAINING
Committed To Training Excellence
Through our innovative learning approach, Clintech Solution equips our students with the latest PG Diploma in Clinical Research Training content, delivered with insightful methods, ensuring that you are not just well-prepared academically but also job-ready. We offer this comprehensive training at competitive prices, making excellence in clinical research education accessible
What we Teach ?
PG Diploma in Clinical Research consists of Clinical Research, Clinical Data Management, Pharmacovigilance & Clinical Trial Data Analysis Using SAS training for 6 months.
Clinical Research Associate (CRA)
The module is designed to provide students with a comprehensive training program tailored specifically to prepare them for the role of a Clinical Research Associate (CRA), aligning with the highest industrial standards. It covers all the essential responsibilities and tasks that CRAs are expected to handle in the real world.
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Clinical Research
(CR)
This module aims to equip aspiring professionals with a robust comprehension of the key aspects related to designing and deciphering clinical trials. It will elucidate the core principles underpinning comparative clinical trials used to assess treatment effectiveness, efficacy, and safety. Furthermore, it will highlight the advantages of clinical trials compared to other study methodologies
Clinical Data Management
(CDM)
This module will delve into matters concerning the continuous data monitoring within a study. It aims to ensure that there is an adequate amount of data available to reliably address the trial's objectives without enrolling more patients than required or subjecting them to undue risks. In this context, the module will place a significant emphasis on the ethical considerations when determining whether to continue enrolling patients in trials
Learning Objective
Clinical Research Process
Planning a Clinical Trial
Preparing essential documents: Protocol, CRF, IB, ICD
Trial Monitoring
Data Entry
21 CFR part 11
ICH E9
SAS Base & Clinial Data Analysis
EC & Regulatory submission
Trial Management
SAE Reporting
Database design
Data Validation
Hands on experience with Open Clinica
SAP