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Klinisch onderzoek

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Ontdek op deze pagina een uitgebreid aanbod van cursussen over klinisch onderzoek, ideaal voor iedereen die wil leren hoe klinische studies worden ontworpen, uitgevoerd en geanalyseerd. Of je nu een beginnende onderzoeker bent die de basisbeginselen van klinisch onderzoek wil begrijpen of een ervaren professional die zijn expertise wil uitbreiden in specifieke gebieden zoals biostatistiek of klinische data management, onze cursussen bieden de wetenschappelijke inzichten en praktische vaardigheden die je nodig hebt.

Je vindt hier cursussen die je leren over de ethische en regelgevende aspecten van klinisch onderzoek, het ontwerpen van klinische proeven, en methoden voor effectieve data-verzameling en -analyse. Leer alles over het opzetten van klinische proeven, het waarborgen van patiëntveiligheid, en het interpreteren van onderzoeksresultaten voor publicatie en beleidsvorming. Deze cursussen bieden ook diepgaande kennis over het gebruik van technologische hulpmiddelen zoals elektronische data capture (EDC) systemen en de nieuwste software voor statistische analyse.

Of je doel nu is om deel te nemen aan baanbrekende medische onderzoeken, je carrière te bevorderen in biomedisch onderzoek, of om beleid en praktijken te beïnvloeden op basis van wetenschappelijk bewijs, onze cursussen bieden praktische begeleiding en deskundige instructies. Je leert van ervaren klinisch onderzoekers en academici die hun expertise delen door middel van interactieve lessen, case studies, en hands-on projecten.

Onze cursussen in klinisch onderzoek zijn toegankelijk voor deelnemers van alle professionele niveaus en bieden flexibele leertrajecten die kunnen worden aangepast aan jouw specifieke onderzoeksinteresses en professionele doelen. Aanvullende bronnen zoals toegang tot professionele netwerken, voortdurende educatieve ondersteuning, en updates over de nieuwste trends en regelgevingen in klinisch onderzoek kunnen je leerervaring verder verrijken en je voorbereiden op succes in de complexe en dynamische wereld van klinisch onderzoek.


Overzicht cursussen Klinisch onderzoek


Doelgroep: Alle niveaus..

Type Opleiding: online/e-learning     Taal: Engels     Duur: 1,5 uur in totaal     Partner: Udemy     Instructeur: Dr. Vincent Baeyens    

Complete Certified Course on Implementing and Applying mandatory CTR for EU and non-EU Clinical Research Professionals.
Wat je leert: Gain an overview of the Clinical Trial Regulation (CTR) to conduct trials in the EU , Understand why changes to the Directive 2001/20/EC were made , Learn and understand the timeline for CTR introduction and transition period
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Doelgroep: Voor beginners..

Type Opleiding: online/e-learning     Taal: Engels     Duur: 1 uur in totaal     Partner: Udemy     Instructeur: Project Upskill    

Introduction to Business Operations in Drug Development & Clinical Research Process.
Wat je leert: Know what are core activities carried out in each phase of the project and their importance , Understand the roles and responsibilities of different business functions in the drug development process , Understand core strategic and project management aspects of business operations
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Doelgroep: Voor beginners..

Type Opleiding: online/e-learning     Taal: Engels     Duur: 1 uur in totaal     Partner: Udemy     Instructeur: Deepika Khedekar    

Introduction to Trial Design & Management with Case Studies.
Wat je leert: Foundations of Clinical Trial , Designing a Clinical Trial - Step-By-Step Process , Conducting a Clinical Trial - Step-By-Step Process
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Doelgroep: Voor experts..

Type Opleiding: online/e-learning     Taal: Engels     Duur: 1,5 uur in totaal     Partner: Udemy     Instructeur: Mahesh Pratapwar    

Clinical Research, Course Overviw, Clinical Trials, Phases of CT, IRB, ICF, Role of IRB, Study Protocol.
Wat je leert: To know about Pharmaceutical Research , To know about how Drug products get discovered , To know basic aspects of clinical research
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Doelgroep: Voor experts..

Type Opleiding: online/e-learning     Taal: Engels     Duur: 9,5 uur in totaal     Partner: Udemy     Instructeur: SG Pharma Trainings    

Glossary and Abbreviations, Guideline, DMP, CRF, Discrepancy Management, Tools for CDM.
Wat je leert: Introduction of CDM , Glossary and Abbreviations , Guidelines for CDM
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Doelgroep: Voor beginners..

Type Opleiding: online/e-learning     Taal: Engels     Duur: 16,5 uur in totaal     Partner: Udemy     Instructeur: SG Pharma Trainings    

Clinical trial Design, Essential documents, Monitoring & Auditing in Clinical Trials & Good Clinical Practice.
Wat je leert: Introduction to Clinical Research , History of Clinical Research , Evolution of GCP
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Doelgroep: Voor beginners..

Type Opleiding: online/e-learning     Taal: Engels     Duur: 3 uur in totaal     Partner: Udemy     Instructeur: Dr. Sachin Potawale    

A Clinical Research Course-ICH-GCP E6(R2), Clinical Trials, Essential Documents, Sponsor, Investigator, Pharmaceuticals.
Wat je leert: Basic understanding of Clinical Research , Historical background of US Drug Law and Regulations , Drug approval process in USA, New drug development-Preclinical Steps, IND, NDA, ANDA
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Doelgroep: Anyone wanting to learn more information about clinical trials..

Type Opleiding: online/e-learning     Richtprijs: €19.99     Taal: Engels     Duur: 32 minuten totaal     Partner: Udemy    

Hello and welcome to my 10th udemy course!And this course we're going to be going over all topics on participating in a clinical trial.Everything from finding a clinical trial to what studies I recommend participating in ,what to bring and what a typical study is like.Also be giving some bonus tips along the way that I have yet to find an any review or talk on clinical studies.(Disclaimer) I am no
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Doelgroep: Clinical Research Associates looking to expand their knowledge,Individuals preparing to test for a clinical research certification,Experienced clinical professionals looking to brush up on regulations,Medical Device Project Managers that need to unde..

Type Opleiding: online/e-learning     Richtprijs: €89.99     Taal: Engels     Duur: 2 uur in totaal     Partner: Udemy    

This course takes the painfully dry regulations and methods used for clinical trials on medical devices and distills them nicely into a clean overview over the course of an hour. Students will learn about Good Clinical Practices (GCP's) and the regulations that govern clinical trials in the USA and rest of world, such as 21 CFR Parts 50, 56, and 812 and the ICH guidelines. As a "quick hit" to gain
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Doelgroep: The course on Stem Cell Research and Therapies is intended for patients and their families and friends who need to find more information about stem cells, who wish to learn how to find relevant information online, and how to work with publicly availa..

Type Opleiding: online/e-learning     Richtprijs: €19.99     Taal: Engels     Duur: 1,5 uur in totaal     Partner: Udemy    

Survival guide to stem cell research and therapies provides comprehensive guidance to publicly available resource materials, libraries and registries for people who are interested in understanding currently available treatment options involving human stem cells.POTENTIAL: The first section explains how stem cells are currently used in research, drug testing, and therapy, and how they have to be ma
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Doelgroep: Anyone interested in SAS Clinical Data..

Type Opleiding: online/e-learning     Richtprijs: €189.99     Taal: Engels     Duur: 2 uur in totaal     Partner: Udemy    

What is Clinical Data?Clinical data is a staple resource for most health and medical research. Clinical data is either collected during the course of ongoing patient care or as part of a formal clinical trial program. Clinical data falls into six major types:•Electronic health records.•Administrative Data•Claims Data•Patient/Disease Registries•Health Surveys•Clinical trials Data
Ele
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Doelgroep: Anyone working within clinical research and involved in the consent process..

Type Opleiding: online/e-learning     Richtprijs: €29.99     Taal: Engels     Duur: 31 minuten totaal     Partner: Udemy    

This course will enable participants to have an understanding of the background and practical implications of the valid informed consent process. The knowledge and understanding gained, coupled with practical examples is intended to give participants the confidence to take a proactive role in the consent process back in the workplace.
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Doelgroep: This Course is designed for all Students and Professionals...

Type Opleiding: online/e-learning     Richtprijs: €34.99     Taal: Engels     Duur: 5,5 uur in totaal     Partner: Udemy    

Clinical Data Management (CDM) is an important phase in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials.CDM assures collection, integration and availability of data at appropriate quality and cost. Clinical Data Management supports the conduct, management and analysis of studies across the spectrum of clinical research. SAS
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Doelgroep: Life Science, Pharma, Nursing, Medical and Clinical Research Professionals..

Type Opleiding: online/e-learning     Richtprijs: €54.99     Taal: Engels     Duur: 1,5 uur in totaal     Partner: Udemy    

This program will help participants to learn Clinical Trial Process/ Clinical Operations. Program starts with an Introduction followed by Phases in Clinical Trial Process, ICH- GCP guidelines, Stakeholders in Clinical Research and their responsibilities in Clinical Trial. Program gives and overview rather an in-depth details. If you are looking to get first hand information about clinical res
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Doelgroep: Professionals seeking a career in Clinical Research,Recent graduates from a science, medical or nursing discipline looking for a job in clinical research,Experienced professionals who want to change their career and take the challenge to work in Clin..

Type Opleiding: online/e-learning     Richtprijs: €54.99     Taal: Engels     Duur: 1,5 uur in totaal     Partner: Udemy     Instructeur: Vera Madzarevic    

This course and workshop will allow you understand the requirements for a clinical research job, as well as identify specific job duties and responsibilities. Completing this program will provide you with a hands on tool to determine your eligibility for a job in clinical research and draw a road map for qualification. The job application process is discussed and a workshop is provided to allow st
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Doelgroep: This course is for anyone woking with clinical research or with a keen interest...

Type Opleiding: online/e-learning     Richtprijs: €24.99     Taal: Engels     Duur: 33 minuten totaal     Partner: Udemy     Instructeur: Linda Hopkinson    

This comprehensive course for Essential Documents will give you all the required information you need regarding documentation required for the conduct of a clinical trial. This course will cover•Define Essential Documents and their purpose  •Understand what ICH GCP E6 R2 says about Essential Documents•Investigate eTMF systems and their place in accurate storage and retrieval of Essentia
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Doelgroep: Freshers who are looking to make career in clinical research industry..

Type Opleiding: online/e-learning     Richtprijs: €54.99     Taal: Engels     Duur: 2,5 uur in totaal     Partner: Udemy     Instructeur: Surabhi Jain    

Basics of clinical research. Learn from the start. All you want to know about clinical research basic. We have divided modules in 7 parts plus a video on drug discovery and development. These module will help you understand various aspects of clinical research. Our course include introduction to clinical research, glossary in 2 parts, ethics committee, regulatory, GCP, Data Privacy and Protection,
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Doelgroep: The target audience for this course is healthcare professionals..

Type Opleiding: online/e-learning     Richtprijs: €69.99     Taal: Engels     Duur: 2 uur in totaal     Partner: Udemy     Instructeur: Sri C    

This course provides an easy understanding of clinical data management and processes involved for generation of high quality clinical trials data that helps in faster commercialization of product Learn Basics Of Clinical Data Management With This Comprehensive Course Get familiar with Clinical data Management  Learn Phases & activities in CDM Identify tools & roles in C
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Doelgroep: Life Science, Nursing, Pharmacy or similar graduates..

Type Opleiding: online/e-learning     Richtprijs: €69.99     Taal: Engels     Duur: 1,5 uur in totaal     Partner: Udemy     Instructeur: Surabhi Jain    

The course would give you a detail of all crucial topics related to Clinical Data Management and it’s basics. The 10 modules would lead to systematically to the depth of each specific subject. At the end you will come out with filled with knowledge about Clinical Data Management which would be extremely useful when you start working in CRO or Pharma companies as clinical research professional.1)
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Doelgroep: Life Science, Pharma or Medical Graduate, Clinical Research and IT Professionals..

Type Opleiding: online/e-learning     Richtprijs: €124.99     Taal: Engels     Duur: 2 uur in totaal     Partner: Udemy     Instructeur: Anuj Tripathi    

Clinical Data Management (CDM) is an important stage in Clinical Research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. Clinical data management helps collection, integration and availability of data at appropriate quality and cost. It also supports the conduct, management and analysis of studies across the spectrum of clini
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Doelgroep: Medical and Nursing graduate students,Postgraduates and PhD students involved with thesis,Research Coordinators involved in Clinical trials,Those in the early stage of their Research Career..

Type Opleiding: online/e-learning     Richtprijs: €149.99     Taal: Engels     Duur: 4,5 uur in totaal     Partner: Udemy     Instructeur: Dr Sabyasachi Sengupta    

Welcome to this course on Clincal Research Methodology. I have designed this course so that even beginners can learn how to do reserch in a methodical way and publish impactful papers. You will come across examples from real research topics in various modules to grasp the subject better. I recommend that you try the "Practice test" before starting the lectures and take the test again after fi
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Doelgroep: Anyone wanting to get into the Life Science / Pharmaceutical industry and looking to work in this field,Want to take up a job as a Clinical SAS Programmer in a Pharma company or a CRO (Contract Research Org.),Want to just play with data using the SAS..

Type Opleiding: online/e-learning     Richtprijs: €199.99     Taal: Engels     Duur: 2 uur in totaal     Partner: Udemy     Instructeur: Aslam Khan    

This course gives an introduction to the Pharmaceutical/ Life Science industry in a simple and visual style that is easy to understand. It shows how SAS is used as a tool to work with the vast amount of clinical data within this industry. The course takes you through an example clinical study sample data, and generate various Clinical Study Reports that are submitted to the FDA (in the US) or othe
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Doelgroep: The course Clinical Research for Beginners is ideal for recent graduates as well as experienced professionals in science, medicine and allied discipline who are looking into career in clinical research,Graduates from other areas are encouraged to att..

Type Opleiding: online/e-learning     Richtprijs: €189.99     Taal: Engels     Duur: 1,5 uur in totaal     Partner: Udemy     Instructeur: Vera Madzarevic    

Have you ever wondered what it takes to land a job in clinical research? First, you have to know what clinical research is all about and the potential jobs, and this course will give you that.This course will provide you with the essentials of clinical research in a very summarized and concise manner to understand the process and to work towards building your qualifications for a job. You will lea
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