Study Conduct
You can bring your own research team to the CIU trials clinic or contract the CIU team to perform the study conduct/ on-site activities.
At CIU, a team of professionals of Study Nurses and Study Assistants are at disposition for on-site study coordination and to perform any type of study visit.
– Pre-screening and checking of eligibility criteria
– Organization and coordination of study visits, including establishing dedicated trials clinics
for particular trials or for multiple trials within a clinical department
– Conduct of study visits:
- Collection and recording of study data according to study protocol
- Obtaining, processing, storage and shipment of biologic samples
- Dispensing and administering investigational medicinal products
- Support study participants with use of interventional medical device
- Document study data in the Case Report Forms, both paper and electronic.
- Identifi
- Identifying, documenting and reporting adverse events according and perform safety reporting
Have you been caught short of staff?
Specific tasks such as conducting entire or partial study visits, or administrative work can be contracted to CIU as a quick fix or for longer periods. We provide study nurse backup for teams where staff members are on leave. Additionally, we are here to assist with training of new staff, mentoring and professional development.
We are here to support your trial, please contact us for further information.