Clinical Research Coordinator
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Study coordinator at CHU Brugmann, Brussels.
-Management of clinical studies from the beginning to the end
-Pre-selection visits, initiation visits, monitoring with CRA’s, close-out visits
-Worksheets elaboration for each visit, administration of study binders and patient’s data
-eCRF (Inform, Rave, OCRDC, Lincoln, Oracle…) and queries resolution
-Safety submission to ethics committee
-First point of contact for principal investigator (PI) and patients
-Translation of inform consents (for academic studies)
-CRA activities for internal academic clinical studies and eCRF elaboration with redCAP.
-Statistical analyses (for academic studies done at CHU-Brugmann)
-Experience on more than 75 clinical studies in oncology, psychiatry, neurology, cardiology, immuno-allergology, palliative care.
GCP – IATA certificate
Study coordinator at CHU Brugmann, Brussels.
-Management of clinical studies from the beginning to the end
-Pre-selection visits, initiation visits, monitoring with CRA’s, close-out visits
-Worksheets elaboration for each visit, administration of study binders and patient’s data
-eCRF (Inform, Rave, OCRDC, Lincoln, Oracle…) and queries resolution
-Safety submission to ethics committee
-First point of contact for principal investigator (PI) and patients
-Translation of inform consents (for academic studies)
-CRA activities for internal academic clinical studies and eCRF elaboration with redCAP.
-Statistical analyses (for academic studies done at CHU-Brugmann)
-Experience on more than 75 clinical studies in oncology, psychiatry, neurology, cardiology, immuno-allergology, palliative care.
GCP – IATA certificate
