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​

• 6 years of clinical research experience in onco-haematology covering activities as such

  • Clinical project assistant (ICF review, protocol review, POS redaction, CRF guidelines redaction, tools creation for CRA) (6 years)

  • Training of CRAs, CTAs, Project Managers on the of electronic case report form

  • Clinical trial monitoring (5 years) in France & Belgium

  • Pharmacovigilance  (2 years) covering queries, reconciliation, case declaration and follow up, management of safety database

• 1 year as case report form administrator (CRF design, CRF qualification )

Experience

• Stem cell autograft & chemotherapy - Phase III in Myeloma (22 sites in France & 4 in Belgium)