Study Nursing
Our study nurses support investigators by conducting trials in accordance with ICH-GCP at the investigative site. The study nurse is the key liaison between the patient, investigator, and the clinical research organization (CRO). Other important functions include organizing and coordinating qualification- and initiation- visits as well as organizing regular monitoring-visits.
A study nurse's duties and responsibilities include:
- Providing intensive patient care
- Scheduling and conducting patient visits
- Submitting applications and reports to authorities
- Handling study drug and laboratory samples
- Conducting trials according to protocols
- Managing source and other documentation
- Communicating and interacting with the investigator and monitor
The IFS supports clinical trial offices in the following departments:
- Cardiology and Pneumology
- Hematology and Oncology
- Gynecology and Obstetrics
- Neurology
- Dermatology, Venereology and Allergology
- Ophthalmology Neurosurgery
To learn more about Study Nursing at the IFS, please contact:
Melanie Querfurt – Head of Study Nursing
Phone: ++49 (0) 551 - 39 - 5669
Fax: ++49 (0) 551 - 39 - 6196
E-Mail: querfurt.ifs@med.uni-goettingen.de