This two-day course will train you in the basic yet crucial areas of clinical monitoring.

28 & 29 Mar and 10 & 11 Oct 2017. Munich Germany.

Clinical Research Training Junior CRAs

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Clinical Research Training Junior CRAsFocussing on the different phases of the life cycle of a clinical trial, all typical tasks of a Clinical Research Associate (CRA) will become clear to you, from selecting the investigators until study site close-out, with a great focus on the “monitoring practice”.

This course is specifically designed for people who have between zero to twelve months’ experience.

It is strongly recommended to have previously attended a training on “Good Clinical Practice (GCP)”, as the aim is to teach how a CRA implements GCP requirements into the daily monitoring tasks.

Interactive workshops with sample protocol and case report forms (CRFs) will introduce participants to the typical and required operations of clinical research from start to finish.

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PROGRAMME HIGHLIGHTSIntroduction to clinical research

Overview of the applicable legislation

The life cycle of a clinical trial

Monitoring activities at different stages

Trial documents and trial management in practice: study subject recruitment & management, source data verification, investigational product management, safety reporting, clinical data monitoring and quality assurance

LEARNING OBJECTIVES✓ To understand the basics and phases of clinical research

✓ To be familiar with expected job tasks of a CRA from the

start to the end of a clinical trial

✓ To comprehend trial documentation

Barbara has been working in clinical operations for 12 years. She is able to provide valuable practical, real life, advice in all areas of clinical study management and GCP. Coming from a CRA background and with CRO and sponsor experience she can shed light on all aspects of clinical operations. Her particular focus is on the creation of systems in clinical operations, and to enable her clients to adhere to the standards.

Training and compliance are her new adventures that she feels very excited about. In her spare time she roams the fields and mountains of Europe on a historical or photographical mission.

All her courses take place in beautiful Munich, in southern Germany.

Course instructor Barbara Gastl

OTHER COURSES BARBARA TEACHES

Clinical Project Management

Clinical Research Training for Senior CRAs

Ich-Good Clinical Practice Training

Clinical Research Training for Clinical Trial assistants (CTAs)

Find out more here

The ECCRT Team +32 2 892 4000