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Summary

experienced Research Scientist (pharmd, phd).
currently studying at the ku leuven to get his Economics/management degree.

Experiences

Current Experience

  • Part-time student


    Since September 2013

Past Experience

  • Sabatical leave

    October 2012 --- September 2013

  • Senior Scientist Pharmacokinetics - Dept of Pharmacology

    November 2008 --- September 2012
    * provide Expert advice on Pharmacokinetics (pk) and Pharmacodynamics (pd) of therapeutic Proteins (nanobody® technology), including modelling and Simulations support; * Planning, designing, monitoring, analyzing, reporting and presenting results of non-clinical pk/pd studies; * interfacing/collaborating with other departments including bioanalytics, In Vitro and In Vivo pharmacology, Toxicology, cmc, Biostatistics, Clinical operations, and Regulatory Affairs; * liaise with external collaborators/researchers at academic institutions and cros; * efficient Communication with project managers with respect to design, timing, resources and follow-up of ongoing studies, including timely and concise interpretation and Communication of topline results; * provide “Competitive Intelligence”, including follow up of applicable regulatory guidelines and industry best practices; * provide input in Health authority briefing packages, ib (investigators brochure), and impd (investigational medicinal product dossier), and responses to ha inquiries; * represent ablynx at scientific conferences (oral or poster Presentations)

  • Principal Scientist / Lead Scientist DMPK

    June 2007 --- October 2008
    *preparation of the Preclinical dmpk Strategy and implementation plan and integration in the global cross-functional development Strategy *preparation of registration and submission documents *provide input to Health authority briefing packages, ib, impd, csd, ccds, and label (spc/uspi), rmp, … *point contact between the department of dmpk and the global compound development team *interfacing / collaboration with other departments including clinical Pharmacokinetics, advanced modeling and Simulations (ams), depts of Bioanalysis and Toxicology, and various centers of expertise (coexp) *provide “Competitive Intelligence” *scientific input / review of dmpk, Clinical pharmacology and Pharmacokinetics protocols, including third party Research proposals / manuscripts *evaluation of in-Licensing opportunities / dossiers and *study Director (sd)/principal Investigator(pi)/study monitor (sm) of In Vitro and In Vivo Metabolism, excretion, and drug-Drug Interaction studies

  • Senior Scientist / Lead Scientist DMPK

    July 2004 --- June 2007
    *preparation of the Preclinical dmpk Strategy and implementation plan and integration in the global cross-functional development Strategy *preparation of registration and submission documents *provide input to Health authority briefing packages, ib, impd, csd, ccds, and label (spc/uspi), rmp, … *point contact between the department of dmpk and the global compound development team *interfacing / collaboration with other departments including clinical Pharmacokinetics, advanced modeling and Simulations (ams), depts of Bioanalysis and Toxicology, and various centers of expertise (coexp) *provide “Competitive Intelligence” *scientific input / review of dmpk, Clinical pharmacology and Pharmacokinetics protocols, including third party Research proposals / manuscripts *evaluation of in-Licensing opportunities / dossiers

  • Scientist DMPK

    June 2001 --- June 2004
    * study Director (sd)/principal Investigator(pi)/study monitor (sm) of a) absorption, distribution, and pharmacokinetic studies with radioactive (incl. qwba) and non-radioactive drugs and b) toxicokinetic studies in various pre-clinical species as study Director: overall responsibility for the scientific conduct of a study and Compliance of the study with the oecd principles of Good Laboratory Practice as study monitor: coordination and scientific follow-up of outsourced studies (acting on behalf of the sponsor) *management of co-investigators involved in above mentioned studies *pre-clinical Pharmacokinetics representative: close collaboration with the pre-Clinical Development Leader and the lead Scientist in the coordination of projects and the follow-up of departmental tasks.

Knowledge

LinkedIn Assessment :
PharmacokineticspharmacologyPharmacodynamicsDrug DevelopmentIn VitroIn VivoToxicologyAntibodiesPK/PDDrug metabolismModelingClinical pharmacologyBioanalysisBiologicalsBiologicsMedical writingProject ManagementEconomicsMarketingManagement AccountingStrategic Human Resources Leadership

Education

  • in Spanish - Level 4 from Center For Adult Education (The Perspective) in 2015
  • Master Of International Business Economics and Management in from KULeuven in 2015
  • PhD (summa cum laude) in Drug metabolism and Pharmacokinetics from Gent University in 2000
  • Ind. PharmD (magna cum laude) in Industrial Pharmacy from Free University of Brussels in 1997
  • Master's degree (cum laude) in Pharmaceutical Sciences from Free University of Brussels in 1995

Area / Region

Gent

Others

Driving License
  • Yes

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