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Experiences

Current Experience

  • Freelance Contractor Senior Regulatory Project Manager


    Since July 2014

  • Freelance Contractor Senior CRA


    Since May 2014
    CRA Senior CRA for Belgium and Netherlands

  • Executive Director and Senior Consultant


    Since November 2013
    Business Development Responsible for Business Development of training portfolio provided by Innovara in Europe and Growing Markets. Those are tailored made Sales and Marketing trainings for Healthcare mainly. More information can be found on www.innovara.com You can contact me for more information on serge.dehon@innovara.com Trainer for the following programs :(please contact me for more information) - Executive Coaching to Advance Medical Presentation Skills : ECAMP: Executive Coaching to Advance Medical Presentation Skill is the world's premiere program which intensively individualizes the development of the specialist's presentation skills through individualized, personal Executive Coaching. - Foundations for Medical Scientific Liaisons™ ("FMSL") : is an intensive 3 day open seminar covering key competencies and functions of Medical Scientific Liaisons (MSLs) with focus on functional competencies, communications and value-added skills that are essential to all MSLs. The purpose of this seminar is to provide a foundational understanding of the key activities, roles, responsibilities and requirements of the MSL, including how the MSL function works internally across the healthcare company and with external medical customers and organizations. - From Clinical Research to Publication : From Clinical Research to Publication (“CRP”) is an intensive, yet thoroughly enjoyable, practical 1.5 day workshop for medical professionals, that explores how to create an appropriate publication based upon the type of research that has been done. In addition, the program addresses decisions that must be made prior to commencing research, such as which form of research to do and types of publications most appropriate for such research. It gives important insights on how to create and submit an abstract, and also gives hands-on practice on to prepare and present a Poster.

  • Freelance Medical Science Liaison


    Since January 2012
    Clinical Development General: - Adhere to client corporate compliance in all activities, including those related to clinical trials, scientific presentations, and responses to unsolicited requests for information. - Maintain clinical, scientific, and technical expertise in specific therapeutic areas; review scientific journals, attend scientific and key technical meetings. - Represent the Medical Affairs organization to investigator community - Maintain ongoing long-term collaborative relationships with investigator and thought leader communities Clinical trial support: - Interact with client Medical Directors and their designees to determine and coordinate health care practitioner, researcher, and investigator activities.. Act as the conduit between external customers and the client Medical Directors. Customer/Investigator support: - Respond to and document unsolicited requests for information on client marketed products and products in clinical development - Represent client products at medical information exhibits during scientific symposia. - Facilitate investigator and thought leader interactions with client Medical Directors Commercial support: - Provide internal clinical input and training to Commercial functions within regulatory guidelines - Provide clinical and scientific support for Advisory Boards - Content development/scientific review of content and presentation materials, upon request And many more.....

  • Founder and CEO of EMEACR;Freelance Consultant


    Since November 2011
    Clinical research Europe, Middle East & Africa/Asia Clinical Research (EMEACR) is a Full Service CRO providing clinical trial services to the pharmaceutical, medical device and biotech companies in Europe, USA and Emerging Markets. EMEACR is headquartered in Dubai, UAE with an operational office in Belgium, headed by a management team with extensive experience within the clinical research environment. We are able to cover Worldwide studies from Phase 1-4 and also BEBA studies. Our mission at EMEACR, as leading CRO in Emerging Markets regions, we believe in developing clinical trials in Emerging Market region in addition to Europe, because it means better treatments and better access for patients in that region as well. We want to contribute in improving patients’ life, by helping and encouraging the pharmaceutical/biotech and medical device companies to develop their novel life saving drugs in the Emerging Markets. With EMEACR, Drug Discovery companies finally found a reliable CRO partner with which they can perform their clinical trials in those Emerging Markets in Africa, Middle East and Asia in addition to Europe. We can put in place an organization, thanks to our LOCAL and REGIONAL EXPERTISE, ensuring that patients remain the central point and that the study timelines are met. EMEACR was built with the spirit of being a reliable service provider. It means that our role is not only limited to execution, but we also advise and guide our clients on the best way to conduct their studies in those Emerging Markets, taking into account the local specificities. Our vision is to become the reference CRO specialized in conducting clinical research in Europe and Emerging Markets, offering state of the art quality services, and cost effective solutions. We strive to employ people with genuine expertise in the region and with a passion for excellence. We offer a dynamic and stimulating working environment; with good opportunities for career development in a growing, innovative company.

  • Freelance Trainer for EMEACR Academy


    Since July 2011
    Clinical research Deliver high quality trainings in Clinical Research for several companies involved in training and e-learning modules. Please visit www.emeacr.org to discover more.

  • Member


    Since January 2010
    Member Active member of BeCRO

  • Shareholder


    Since January 2008
    CEO Managing 3 game shops in Belgium with my wife who is taking the active CEO lead of those 3 shops located in Maasmechelen / Sint-Truiden and Lommel. www.gamestars.be Including Webshop soon.

  • Clinical Research Consultant/Manager


    Since January 2005
    Clinical Research Consultant Project Management/ Clinical Research Consultant in Belgium, Netherlands, France, UK, Switzerland and many more countries.

  • Founder & Chief Executive Officer & Freelance Consultant


    Since January 2005
    Clinical Research Consultant Experienced Clinical Research Consultant/Manager Experienced EU Regulatory submission Consultant. Belgium, France, Netherlands, UK, Switserland(French part), India. Interested in emerging countries clinical research(Middle East/Africa/AsiaPac and LatAm). Associate Trainer for Institute of Clinical Research

Past Experience

  • Freelance Senior CRA

    April 2013 --- December 2013
    Medical Device

  • Freelance Senior CRA / Study Start-Up Specialist

    April 2011 --- February 2013
    CRA

  • Outsourced Senior CRA

    May 2009 --- January 2010
    Phase 3

  • Senior Consultant

    October 2004 --- July 2009
    Internet

  • Global Trial Leader

    November 2008 --- June 2009
    Phase 3

  • Outsourced Embedded Project Manager

    July 2008 --- November 2008
    Phase 3

  • Outsourced Senior CRA

    February 2006 --- September 2008
    Phase 3

  • Clinical Trial Consultant

    January 2004 --- January 2005
    oncology

  • Sales & Marketing

    January 2000 --- January 2003
    Diagnostics

  • Outsourcing coordinator

    January 2000 --- January 2000

  • Project Manager

    January 1996 --- January 1999

Personality

Self Assessment :
FlexibilityAttention to detailCollaborationCommunicativeCreative thinkingCritical thinkingInterest in knowledgeOptimismProactivityProblem solvingService orientedStrategic thinkingTrust

Knowledge

LinkedIn Assessment :
Clinical Research ConsultancyEMEA RegionClinical trialsVaccinesRegulatory submissionsCROGCPClinical researchProblem SolvingClinical trial managementClinical monitoringICH-GCPInfectious diseasesClinical DevelopmentPharmaceuticalsClinicalCardiologyHealthcareMedical DevicesoncologyDermatologyMedical writingCTMSRegulatory affairsBiotechnologyClinical Data Management (CDM)GastroenterologyQuality Assurance (QA)InformCoachingprotocol developmentTeam BuildingStrategic PlanningPediatricsNew Business DevelopmentProcess improvementTraining & DevelopmentStaff TrainingTraining DeliveryEntrepreneurial SkillsAfricaMiddle EastPhase IStudy DesignElectronic Data Capture (EDC) Pharmaceutical IndustrySOPRegional Medical Science LiaisonPharmacovigilanceTherapeutic Areas

Education

  • Master in Chemistry in Clinical Research from Katholieke Universiteit Leuven in 1993
  • in 8u Mathematics from Sint-Jorisinstituut in 1990
  • in from Johannes Paulus II in 0000

Training and Certification

  • Certified Trainer ECAMP in 0000 Certification
  • MICR in 0000 Certification

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
French
Full Proficiency
English
Full Proficiency
German
Elementary Proficiency

Work Preferences

  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    BrightOwl freelancer
  • International:
    Yes

Area / Region

Belgium

Others

Driving License
  • No

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