Clinical Research Associate (m/f)

REFERENZNUMMER:

342986/11

IHRE AUFGABEN:

-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

IHRE QUALIFIKATIONEN:

-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

WEITERE QUALIFIKATIONEN:

CRA