Online PG Diploma In Clinical Research​
ONLINE | CLASSROOM | CAMPUS TRAINING
Committed To Training Excellence
Clintech Solution empowers our students to become job-ready by offering the most up-to-date Online PG Diploma in Clinical Research course content, delivered with insight and an innovative learning approach, all at competitive prices.
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At Clintech Solution, we provide an innovative online learning approach that enables our students to effectively apply the theoretical knowledge and skills acquired during our online courses in the clinical research industry
What we Teach ?
The Online PG Diploma in Clinical Research spans six months and covers an array of essential subjects, including Clinical Research, Clinical Data Management, SAS for Clinical Data Analysis, and Pharmacovigilance training
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 Trail Management
(CTM)
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
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
Pharmacovigilance
(PV)
This module equips aspirants with an understanding of the complex landscape concerning the risks and benefits associated with drug use in humans. It encompasses the causes, manifestations, and consequences of adverse drug effects (ADEs), as well as the methods for their detection and monitoring. Furthermore, it explores the historical and legal frameworks related to this critical aspect of healthcare.
SAS For Clinical Data Analysis
Our SAS training is meticulously crafted to instruct students in the application of SAS programming skills within the context of clinical trials. SAS Clinical training provides the knowledge and expertise necessary to ensure that clinical data adheres to established standards, facilitating its use for strategic analysis.
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