My professional path as a project manager has been varied and progressive in complexity and leadership.
At a local or country level, I was responsible for clinical study set-up, protocol and safety follow-up, and recruitment targets. At a global or sponsor level, I worked articulating cross-functional clinical teams, developing clinical studies in diverse disease areas and having them implemented by local teams. I then expanded my expertise area outside of clinical development by becoming responsible for the functional management of global Epidemiology and Medical Affairs teams. I supervised a team focused on scientific engagement and Market Access. Since then I also successfully supervised a senior issue management team, supported the project management office on the full project costing exercise and delivered training to newcomers in the team.
My new challenge is now to fully integrate my technical, leadership and strategic knowledge into value management framework for the Measles, Mumps, Rubella and Varicella (MMR,V) program.
Senior Program ManagerBrussels, Belgium
Since October 2017
Matrix management of cross-functional, multi-disciplinary team.
Senior Project ManagerMarch 2016 --- September 2017
Medical Project Manager BrusselsJanuary 2014 --- February 2016
Global Study Manager (Novellas Healthcare consultant)October 2010 --- January 2014
Regional Study Manager (Novellas Healthcare consultant)February 2013 --- July 2013
Product ManagerJune 2010 --- August 2010
Chemical Products: Antioxidants and Organic Minerals
Clinical Research Associate (CRA)January 2010 --- May 2010
Clinical Research Associate (CRA)September 2009 --- December 2009
Clinical Research Associate (CRA)December 2007 --- August 2009
Clinical Research Associate (CRA)January 2007 --- January 2008
Clinical Data Manager (DM)January 2006 --- January 2007
Main Analyst Enter LocationJanuary 2001 --- January 2005
Chemistry TeacherJanuary 2000 --- January 2001
Chemistry TeacherJanuary 1999 --- January 2000
Project ManagementInformed Consent ProcessMonitoring Study ProgressManaging Clinical Trial SuppliesGood Clinical Practice (GCP)Knowledge of the drug development processCapacity ManagementContractingContingency WorkersQuality ManagementLaboratory Management BiochemistryBiotechnologyCAPAClinical DevelopmentClinical operationsWriting Study Procedures and SOPsVerificationSOPClinical trial managementData ManagementMicrosoft OfficeProblem-solving methods and troubleshooting
Skills and Expertise
PMPproject managementBudget managementtime managementScope Manangementchange managementRisk ManagementBusiness strategyBusiness planningBusiness operations
Master of Science (MSc) in Applied Chemistry - Biotechnology from Universidade Nova de Lisboa in 1998
12th degree (A-levels) in Natural Sciences from Escola Secundaria Jose Gomes Ferreira in 1992
Training and Certification
Project Management PMP® preparation course - Basic + Exam program; Xenturion, Brussels in 2014 Training
Manage Others; The Clinical College, Brussels, Belgium in 2013 Training
Project Management Professional - PMP® in 2015 Certification
Project Management Professional (PMP)® in 0000 Certification