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Study Nurse Training
To learn more about our programs and customized training options, or request a free proposal, contact us to discuss your needs and desired goals.
Course overview
This basic course imparts medical professionals the additional qualification ‘Study Nurse’
This 5-day intensive program teaches the basic principles of clinical research, and gives a thorough insight into how clinical trials are conducted in hospitals and doctors’ practices. It focuses particularly on the recent developments in the field of clinical research and the latest legal and regulatory guidelines (ICH-GCP/AMG).
Please note that due to the current situation we reserve the right to postpone courses and events at short notice.
Course details
€1200,00 + VAT (incl. Lunch & Beverages)
Program Fees
5 days
Duration
German
Language
Aim
Participants
Your benefits
Program Overview
Contact
Aim
The practical nature of the course means that you will be familiar with all standard study documentation, and be able to perform all the tasks required of you in your daily work as a Study Nurse.
On completion of the seminar you will receive a certificate that is recognized within the clinical research industry.
The German Association for Study Nurses and Study Coordinators (BUVEBA) was founded in 2011 in order to define the training requirements and qualifications for Study Nurses nationwide. Every year the Association hosts the Federal Congress for Study Nurses to link its members and to discuss current topics within the profession. You can find more information about the Association and its activities at BUVEBA.de.
Participants
Professional and well-trained study teams are key to ensuring that clinical trials are carried out in accordance with national and international guidelines. As the primary contact for patients, Investigators and Clinical Monitors, Study Nurses play a central role in clinical research. They ensure that everything runs smoothly at the site. They look after subjects, collect and record relevant study data and prepare for monitoring visits and audits. This course equips you for all of these tasks and keeps your knowledge and skills up-to-date.
Your benefits
Professional and well-trained study teams are key to ensuring that clinical trials are carried out in accordance with national and international guidelines. As the primary contact for patients, Investigators and Clinical Monitors, Study Nurses play a central role in clinical research. They ensure that everything runs smoothly at the site. They look after subjects, collect and record relevant study data and prepare for monitoring visits and audits. This course equips you for all of these tasks and keeps your knowledge and skills up-to-date.
Program Overview
- Introduction to clinical research
- Guidelines
- Regulatory framework
- International Ethical Principles and Guidelines Ethical considerations and
- Competent Authorities
- Roles and responsibilities according to ICH-GCP
- Protocol, Patient information, Investigator’s Brochure
- Case Report Forms (CRFs)
- Source data – Requirements of medical records
- Investigator Brochure
- AE / SAE – Safety data
- Study medication
- Laboratory
- Types of monitoring visits
- Audits
- Study coordination
Contact
Additional prepackaged courses
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Clinical Research Associate Fundamentals
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GCP for Investigators
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Statistical Aspects of Clinical Trials
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Project Management for Clinical Trials
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Good Clinical Practice: Conducting Clinical Trials
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Business English for Clinical Trials
Get started today
We develop tailored, meaningful and effective education and training programs to meet the
increasing demand for professionals and executives in the biopharmaceutical industry. To learn more about our programs and customized training options, or request a free proposal, contact us to discuss your needs and desired goals.
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