I’m offering freelance CRA services in Finland through my own company Clindoc Ltd.
I have more than 10 years of experience in monitoring Phase I-IV clinical trials, including global multicenter trials and local academic trials.
My main therapeutic experience is in Oncology, Urology, Gynaecology, Hematology and Internal Medicine.
- site evaluation and selection
- preparation of regulatory and ethics committee submissions
- study agreements management
- study financial administration
- study coordination
- site management and monitoring including site initiation, monitoring and close out
- audit preparation, participation and follow-up
- site staff training and mentoring
- GCP training