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pierre is a biometrics professional with 15 years experience in the Pharmaceutical Industry. he started his Career as a technical professional being a Clinical (SAS) programmer where after he grew in a team leading role for global Statistical programming. after mastering his team lead skills he grew into the ad role. in 2009, pierre joined iddi where he started his role as an ad within Data Management and then gradually grow to being the Director of eclinical services within the company. during these years, pierre learned to communicate with international, multicultural teams. he learned to aim for high quality and performance by being a true Leader. moreover he knows exactly how to deal with difficult situations, face demanding clients and meeting challenging deadlines. although the technical background, pierre hasn't been hands on involved with the programming itself. his strengths are more focused on coordination, Planning and budget management. pierre is looking for a new exciting role where he can use his (project) management skills. he is keen to learn new talents and contribute to a new company as a valuable asset.


Past Experience

  • Director, eClinical Services

    April 2011 --- July 2015

    my main role at iddi was to supervise operational teams providing Data Management & Randomization services. eclinical services goal being to provide top quality support to our clients.

    • managing the eclinical services department employing 30 people and consisting of 3 teams : 1) Randomization systems 2) data managment & edc systems 3) Validation and support (incl. help desk acitvities)
    • responsible for Budgets and plans for the development of the department.
    • directed the development, evaluation and adaptation of processes for providing eclinical services support for Clinical trials (ensuring work is delivered on time to the standards required).
    • Project Management for studies and technical/standardization exercises. 

  • Annual Conference Chair and co-Chair

    October 2012 --- October 2014
    the 2014 was phuse’s tenth annual conference! i chaired this annual event with "data transparency” as main theme. data being at the heart of our activity and transparency being a hot topic at the time, it seemed the most logical theme to select. the 2014 conference was the one with the highest attendance ever and was a great success for the phuse organisation. previously, i co-chaired the 2013 annual phuse conference in brussels with "patient centricity" as main theme.

  • AD & DH Streams (co-)Chair

    October 2009 --- October 2012
    ad: application and Software Development stream covers the development process of Applications and software designed to assist us, directly or indirectly, in our daily job. dh: data handling stream is dedicated to various aspects of data handling and database management done by programmers in the Pharmaceutical Industry.

  • Associate Director, Data Management

    August 2009 --- April 2011
    • management of Data Management team (around 12 people).
    • guidance to team members and coordination of all Data Management activities.
    • management of relationship with clients and external providers.
    • Project Management for studies and technical/standardization exercises.

  • Brussels Single Day Event Chair

    October 2008 --- October 2010

  • Associate Director, Budget/Resource/Vendor Management

    September 2007 --- July 2009

  • Global Statistical Programming Team Leader

    June 2003 --- August 2007
    • responsible for the development and supervision of the global Statistical programming team (be/uk/us) in order to provide Statistical results supporting Clinical study reports.
    • coordination of activities in order to meet deadlines with the expected quality.
    • management of the relationship with external providers (selection and contract Negotiation).

  • SAS Consultant - Clinical Programmer

    April 1999 --- May 2003
    • SAS programming support to Clinical Data Management.
    • management of the clinical programming team (activity and Planning coordination).
    • cleaning/Validation of clinical Databases and creation of ad hoc tables and listings.
    • participation in the development of a data warehouse (ph-dataware).

  • Responsable Secteur Logistique

    August 1998 --- February 1999


Self Assessment :
Problem solvingTrustAnalytical thinkingCoordinationOrganizationAttention to detailSociabilityFlexibility


Self Assessment :
R&DClinical DevelopmentClinical trialsGood Clinical Practice (GCP)Regulatory submissionsPhases of clinical development (phase I to IV)people managementTeam LeadershipCommunication SkillsProject ManagementProgrammingSASClinical Data Management (CDM)Electronic Data Capture (EDC) Randomization SystemsWriting Study Procedures and SOPsHIVHPVHCVoncology
LinkedIn Assessment :
Clinical trialsData ManagementCDISCEDCClinical Data ManagementeClinicalSAS programmingRandomizationSASCROFolk DanceBallroom DanceGCPSOPClinical DevelopmentTherapeutic AreasDrug DevelopmentClinical researchValidation21 CFR Part 11ICH-GCPoncologyPharmaceutical IndustryCTMSLife SciencesSAS programming


  • Master of Science (MSc) in Business Administration and Management, General from Facultés universitaires catholiques de Mons in 1998
  • in from Athénée Royal Jules Bara in 1992

Training and Certification

  • SAS Programmer in 0000 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    associate Clinical Project Manager Clinical Research Associate (CRA) Clinical Trial Manager
  • Work From Home:
  • Work Regime:
    Permanent position
    BrightOwl freelancer
    BrightOwl employee
  • International:

Area / Region

Brussels, Belgium


Driving License
  • Yes

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