Description
We are looking for a
Clinical Research Associate (m/f)
Reference: -en
Start: asap
Duration: 12 MM+
Place: in Basel
Branch: Herstellung von pharmazeutischen Erzeugnissen
Your tasks:
- Perform qualification visits and initiation visits as agreed with the clinical pharmacologist for the assigned studies
- Perform routine monitoring visits and close out visits and assure that the CROs are delivering high quality research
- Identify site issue and ensure resolution
- Report to the study team and the CRO site staff any finding at the monitoring visits by completing monitoring visits reports
- Manage all study supplies and supervise biological sample shipments to bio-analytical laboratories and central laboratories
- Ensure timely completion of the eCRF and identify any discrepancies by reviewing the eCRF data
- Review and provide input on study-related documents and CRO-prepared documents as protocol amendments, contracts, case report forms or clinical study reports
- Responsible for the Trial Master File maintenance
Your qualifications
- University degree in Science or Health related discipline and / or nursing
- Working experience in clinical research in a CRO or pharmaceutical company with experience in monitoring
- Strong ICH-GCP knowledge
- Excellent English skills (written and oral)
- Willing and able to travel in different countries
Skills:
- CRA