After somewhat 6 years spent completing, with strong diligence and ethics, a high-quality scientific project in an international fast-paced environment, I let my never-ending curiosity and inner peace taking my eyes in the backstage of the world during a 2-year journey, holding cultural exchanges off-the-beaten tracks, and embracing challenges one after another, while sustaining my endeavors through various assignements undertook on the go.
A 2-week solo trek to the highest pass in the world (5416m) within the Himalayans...
Though, as improving projects is, and has always been, a major interpersonal mindset of mine, that I own hands-on experience and particular interests in various fields (management, sciences, communication, digital...), I now lay down valuable skills at disposal of businesses eager to thrive in today’s challenging world. Please note that I don't mind aiming something big because that’s where the rewards are; outside the comfort zones.
Senior Scientific Officer
October 2016 --- September 2017
• Conducting comparative scientific and regulatory policy studies in authoritative bodies; • Developing, reviewing, approving technical (SOPs, characterization reports design) & general (company’s scientific opinion and health policy standards) content materials; • Ensuring QA of substance toxicology characterization reports; • Contributing to internal resolution and approval of protocol deviations; • Assisting in the technical framework development of an advanced bibliographic algorithm; • Scouting for enrollment of international Audit Committee members; • Providing digital marketing and communication support;
April 2015 --- March 2017
• Planning and executing a full-cycle international project; • Holding leadership and managerial positions (10+ team members) through temporary assignments; • Tackling challenges within national and international regulations; • Negotiating product acquisitions in foreign languages on a daily basis; • Developing and promoting editorial content materials through multiple digital channels;
Clinical data manager
June 2014 --- September 2014
• Ensuring QA of clinical study databases in accordance with ICH/GCP and SOP guidelines; • Contributing to external resolution of protocol deviations through study site guidance regarding proper usage of Oracle Clinical software (CDISC);
September 2007 --- February 2014
• Fundraising and securing public/private research grants; • Planning and executing a full-cycle scientific project; • Developing, reviewing, approving technical (SOPs, data analysis reports, scientific manuscripts) & general (funding reports, scientific presentations) content materials; • Managing and overseeing workflow and training of 5+ undergraduate students and staff members; • Negotiating product acquisitions; • Complying with scientific ethics;
AdaptabilityEfficiencyCreative thinkingAttention to detailOptimismInnovative thinkingCuriosityCritical thinkingAnalytical thinkingOrganizationCoordinationFlexibilityProblem solvingProactivityResiliencyStrategic thinkingWillingness to compromise
Skills and Expertise
Analytical skills Analyze data execute and publish scientific projects (in biology) Guide students Report dataArchive study documentsAssess adverse reactionsCollect patient forms and questionnairesConduct literature searchesData verificationDevelop and maintain GCP/ICH compliant processes which control the quality of work and clinical trials Ensure consistency between the protocol and CRFEnsure good clinical practice (GCP)Execute scientific projectsOral presentation
Doctor of Philosophy (PhD) in Sciences - Molecular Biology from Université libre de Bruxelles in 2013
Master of Science (MSc) in Sciences - Molecular Biology from Université libre de Bruxelles in 2007
Training and Certification
BioWin - Clinical Trials Training Modules (CRA/CRO; ICH/GCP; regulatory affairs) in 2014 Training
English scientific lessons in 2013 Training
Clinical Trial Modules Certification
Excel VBA Programming Certification