Clinical Research Training for Senior CRAs

Tijdsduur
Startdatum en plaats
Logo van European Centre for Clinical Research Training

Tip: meer info over het programma, startdatum, prijs, en inschrijven? Download de brochure!

Startdata en plaatsen

Brussels
23 sep. 2019

Beschrijving

Clinical Research Training for Advanced CRAs

Course Description

In this two-day course, you will learn how to optimize monitoring methods and skills, how to boost recruitment and how to solve site management issues and gain insights into protocol and CRF development, quality systems and audits. A detailed look at ICH-GCP and updates on the EU directives will also be given and a half-day session on communication skills will address issues such as how to reach a win-win situation with study site personnel and how to work within a team. This course has been specifically designed for people with at least 2 years' experience as a Clinical Research Associate (CRA) and who want to set new goals and…

Lees de volledige beschrijving

Veelgestelde vragen

Heb je een vraag? Onze adviseurs helpen je graag. Bel ons op 085 7440830 of e-mail naar info@springest.nl.

Nog niet gevonden wat je zocht? Bekijk deze onderwerpen: Good Clinical Practice, Laboratoriumtechniek, Medisch, Strategisch onderhandelen en Onderhandelen (verkoop).

Clinical Research Training for Advanced CRAs

Course Description

In this two-day course, you will learn how to optimize monitoring methods and skills, how to boost recruitment and how to solve site management issues and gain insights into protocol and CRF development, quality systems and audits. A detailed look at ICH-GCP and updates on the EU directives will also be given and a half-day session on communication skills will address issues such as how to reach a win-win situation with study site personnel and how to work within a team. This course has been specifically designed for people with at least 2 years' experience as a Clinical Research Associate (CRA) and who want to set new goals and objectives in their career.

Learning objectives

• To refine knowledge of ICH-GCP, quality systems and audits
• To provide an update on EU Clinical Trial Directives
• To highlight important elements in the development of protocol and CRF
• To explain the elements of efficient site management from start to finish
• To develop soft skills for improving communication and teamwork

Programme highlights

• Importance of international research – the role of the ICH process
• Update on the implementation of the EU Clinical Trial Directive
• Protocol development and Final Study Report
• CRF development & Electronic Data Capturing
• Quality systems and audits
• Communication skills (content: see soft skills training part in this prospectus)

Workshops

• Improving recruitment and site management
• Informed Consent
• Audit findings

Comprehension Test (included in the Course Fee)

Who should attend

CRAs with a minimum of 2 years experience who want to set new objectives in their career and/or people working in clinical data processing, biostatistics, regulatory affairs, etc


*Due to unforeseen circumstances, the programme may change and the ECCRT reserves the right to alter the venue or cancel the event.

Trainer: Marleen Verbeeck, PhD & Gerald Van Roey

Language: English

Important: In case you have more than 5 interested participants you can save about 50% of your costs by inviting the trainer over for a tailored on-site training

Blijf op de hoogte van nieuwe ervaringen

Er zijn nog geen ervaringen.

Deel je ervaring

Heb je ervaring met deze cursus? Deel je ervaring en help anderen kiezen. Als dank voor de moeite doneert Springest € 1,- aan Stichting Edukans.

Heb je een vraag? Onze adviseurs helpen je graag. Bel ons op 085 7440830 of e-mail naar info@springest.nl.

Vraag nu gratis en vrijblijvend informatie aan:

Aanhef
(optioneel)
(optioneel)
(optioneel)
(optioneel)
(optioneel)
(optioneel)
(optioneel)
(optioneel)
We slaan je gegevens op, en delen ze met European Centre for Clinical Research Training, om je via e-mail en evt. telefoon verder te helpen. Meer info vind je in ons privacybeleid.