Services
You would like to participate as a study site in a clinical trial!
I would like to support you:
Clinical Study Preparation
- settling into study specific documents
- participation at initiation visits
- participation at study specific trainings
- checkup of study materials
Study Conduct
- patient recruitment using the existing subject data base, e.g. by phone or coverletter
- prescreening of potential participants (by phone or personnel)
- scheduling the subjects according to the protocol, e.g. in cohorts
- ensuring patients are given all the information they need to comply with the study requirments at home
- adminstration, appropiate storage and application of study medication
- conducting of study specicif tests and procedures which must not be performed by an investigator
- transferring of source data into CRF (hardcopy and electronic)
- processing of data clarification forms
- supporting the investigator (e.g. SAE reporting)
Additional Duties
- consulting and training of (study-)team
- maintenance of study files and filling of study documents
- requesting of study medication and/or material
- checkup the return of study medication/material to the sponsor
- communication with the study management and the responsible monitor
- adminstrative support for monitoring visits
- participation at investigator meetings, if necessary