Senior Clinical Research Associate (freelance)
Since September 2014
Pharmacovigilance OfficerSeptember 2013 --- August 2014
responsibilities: processing of spontaneous and study related safety reports, follow-up on queries, Training of new employees.
Scientific advisor respiratoryJanuary 2012 --- August 2014
responsibilities: follow-up on domain specific literature, review of promotional materials, writing of the scientific part of Reimbursement dossiers, medical information, Training of medical representatives, kol management, support of Phase IV trials and all of this in close collaboration with the Marketing department.
Scientific advisor oncology-haematologyJanuary 2012 --- December 2012
responsibilities: same as specified above for Respiratory.
Senior coordinating Clinical Research AssociateMarch 2002 --- December 2011
this role involved the following items in the conduct of Clinical trials: - site selection & feasibilities - budget negotiations & contract handling - Informed Consent writing - trial submission to the ec's - initiation, monitoring & close-out activities - Training & Coaching of junior CRA's i have experience in the following Therapeutic Areas: - gastro-enterology - bone & joint - oncology - Dermatology - urology - Ophthalmology - Cardiology - Vaccines
Clinical Research Associate (CRA)January 2001 --- March 2002
LinkedIn Assessment :
Honour's degree in Bedrijfskunde from Vrije Universiteit Brussel in 2000
Masters in Pharmacy from Vrije Universiteit Brussel in 1999
Area / Region