
Audrey Mabanza
Clinical Project Manager
Master degree’s in biological nutrition with over 6 years experience in clinical research including 2 years in drug safety pre-marketing authorisation applications
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6 years of clinical research experience in onco-haematology covering activities as such
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Clinical project assistant (ICF review, protocol review, POS redaction, CRF guidelines redaction, tools creation for CRA) (6 years)
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Training of CRAs, CTAs, Project Managers on the of electronic case report form
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Clinical trial monitoring (5 years) in France & Belgium
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Pharmacovigilance (2 years) covering queries, reconciliation, case declaration and follow up, management of safety database
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1 year as case report form administrator (CRF design, CRF qualification )
Experience
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Stem cell autograft & chemotherapy - Phase III in Myeloma (22 sites in France & 4 in Belgium)