Antoine Larivée
Clinical Research Coordinator
Deze persoon inhuren
Stuur een vacature direct naar deze kandidaat
Over
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
Ervaring
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
