Description
Clinical Research Knowledgebase is a online repository of Learning content for Clinical Research that covers all the concepts of conducting clinical trials, the global regulations that govern this and key processes in clinical trial management. The extensive repository covers all the domains in clinical research including clinical research operations, clinical data management, pharmacovigilance, medical writing, regulatory affairs and project management. Subscribing to this knowledgebase is a great start for students and professionals that wish to get started in the field of clinical research. Its also a perfect fit for students already enrolled in a clinical research program and would like to get access to quality content that will help you better learn, understand and expand your knowledge. On subscribing to the knowledgebase you get access to all our programs in Clinical Research for a single fee. The courses are delivered via our online learning portal. The following eLearning Programs are included as a part of the subscription
- Introduction to Clinical Research
- Ethics in Clinical Research
- Diploma in Clinical Research
- Diploma in Medical Writing
All Subscriptions are billed monthly and can be cancelled at any time. Subscription to Knowledgebase does not include software access. You can purchase software access at https://www.clinskill.com/software
Topics
Content Stats – 32 Modules, 228 Chapters, 186 Quizzes
Clinical Research
- Module 1 – General Introduction
- Module 2 – Epedemiology and Evidence Based Medicine (EBM)
- Module 3 – Pharmaceutical Medicine
- Module 4 – Therapeutic Areas
- Module 5 – Ethics in Clinical Research
- Module 6 -Roles and Responsibilities
- Module 7 – Clinical Trial Preparation
- Module 8 – Essential Documents and Regulatory Submission
- Module 9 – Study Start-up
- Module 10 – Clinical Trials Monitoring
- Module 11 – Compliance and Audits
- Module 12 – Data Management and Biostatistics
- Module 13 – Regulatory Affairs in Clinical Research
- Module 14 – Medical Device Trials
- Module 15 – Project and Vendor Management
- Module 16 – Financial Management of Clinical Trials
- Module 17 – Personality Development and Communication Skills
- Module 18 – Oracle Siebel Clinical CTMS
Medical Writing
- Module 1 – Introduction to Clinical Research
- Module 2 – Epidemiology and EBM
- Module 3 – Pharmaceutical Medicine
- Module 4 – Basics of Good Medical Writing
- Module 4 – Computer Skills
- Module 6 – Overview of the Regulatory, Marketing and Drug Promotion Process
- Module 7 – Common Technical Document
- Module 8 – Protocol, Investigator’s Brochure and Case Report Forms
- Module 9 – Clinical Study Report
- Module 10 – Sentence Control
- Module 11 – Writing Flow and Cohesiveness
- Module 12 – Publication Writing
- Module 13 – Documents in Medico-Marketing
- Module 14 – Managing the Review Process
Certification
The Knowledgebase gives you access to multiple courses for a single course Fee.
You will be awarded a Certificate of Completion for all the courses in the Knowledgebase for which you meet the course completion criteria.
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