This blended learning course provides experienced monitors with the knowledge and skills to deal with more complex clinical trials

and site management issues

31 Mar and 06 Oct 2017. Munich Germany.

Clinical Research Training for Senior CRAs

Click here to find out more

Clinical Research Training for Senior CRAsDo you want to refresh and improve your CRA skills? Do you need some inspiration to boost your clinical trial monitoring techniques and approach? This blended learning course provides, the experienced monitors, with the knowledge and skills to deal with the more complex clinical trials and site management issues. The face to face training, supported by eLearning, gets the best outcome and you can learn at your own pace.

Through an interactive approach, in this blended learning course, you receive a concise update of the current European clinical trial legislation and you will learn more about clinical trials in developing countries. The critical milestones of clinical trials, contingency plans, dealing with non-compliances, risk-based monitoring, your relationship with the investigator and coaching junior CRAs are the main topics.

Book Here

PROGRAMME HIGHLIGHTSImportance of international research. The role of the ICH process

Questions and Answers on a monitoring plan

Selection of the right investigator

The informed consent: verification of the process

Improving recruitment of study subjects and tips for site staff to enhance subject retention

Upgrading monitoring tasks: prioritizing monitoring activities, accurate monitoring reporting, efficient tracking, dealing with non-compliances

Coaching junior CRAs

LEARNING OBJECTIVES✓Be up-to-date on current European legislative rules✓Manage investigational sites better from screening to

database lock✓Take the right actions to resolve site issues, ascertain

appropriate corrective and preventive actions✓Expand your knowledge and improve your monitoring

skills.

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 Research Training for Junior CRAs

Clinical Project Management

Ich-Good Clinical Practice Training

Clinical Research Training for Clinical Trial assistants (CTAs)

Find out more here

The ECCRT Team +32 2 892 4000