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Summary

challenging a Career in the field of Pharmaceuticals industry. especially in the sector of Clinical research (Clinical operations, medical affairs). desire to work within a dynamic company that allows me to gain more experience through work. good head for responsibilities, initiative, organization and Communication.

Experiences

Current Experience

  • Clinical Lab Planning Coordinator

    Rixensart, Belgique
    Since June 2014

    gsk – global Vaccines Clinical Lab (rixensart) for valesta - Planning monitoring of some studies - monitoring of samples preparation/Testing in collaboration with the Lab study manager in accordance with the due dates - prioritization of the specific instruction redaction, samples reception, and samples preparation - planification of the preparation team work - release of samples to Intern labs according to their workload - follow-up of various process improvements and system remediation - update SOP - consolidate information about the arrival of the first Clinical study samples - support (business, migration Windows, budget…) - metrics (development of workload timesheet and dashboard)

    GSK – Global Vaccines Clinical Lab (Rixensart) For VALESTA - Planning monitoring of some studies - Monitoring of samples preparation/testing in collaboration with the Lab Study Manager in accordance with the Due Dates - Prioritization of the Specific Instruction redaction, samples reception, and samples preparation - Planification of the preparation team work - Release of samples to intern labs according to their workload - Follow-up of various Process improvements and System remediation - Update SOP - Consolidate information about the arrival of the first clinical study samples - Support (Business, Migration windows, budget…) - Metrics (development of workload timesheet and dashboard)

Past Experience

  • Project Coordinator Trainee

    January 2014 --- April 2014
    develop and maintain project schedules; develop tracking tools; calculate metrics; liaise between operational team, management team and client; prepare meeting minutes, Presentations, tables, report; ensure follow-up of all distributed tasks. provide help to other department: Medical writing (Translation and qc of icf; publishing of ich sections 14 to 16); qa (tracking of deviations; update of sops requirements).

  • Pharmacist

    September 2013 --- September 2013
    drug information; check the prescriptions; dispensing ; patient counselling; identifying and resolving drug-related problems; evaluating drug use and patient behaviour to improve Patient Safety; managing the back-office; handling orders ; preparations of the drugs (capsules, cream, suppository,…)

  • Pharmacist assistant

    July 2013 --- July 2013
    drug information; check the prescriptions; dispensing ; patient counselling; identifying and resolving drug-related problems; evaluating drug use and patient behaviour to improve Patient Safety; managing the back-office; handling orders ; preparations of the drugs (capsules, cream, suppository,…)

  • Pharmacist intern

    October 2012 --- May 2013
    drug information; check the prescriptions; dispensing ; patient counselling; identifying and resolving drug-related problems; evaluating drug use and patient behaviour to improve Patient Safety; managing the back-office; handling orders ; preparations of the drugs (capsules, cream, suppository,…)

  • Researcher Internship

    January 2012 --- February 2012
    cellular cultures and use of analytic techniques for tumour cells degradation detection. my project was to evaluate the difference of efficacy between my new Molecule and the usual antitumoral Treatment. and the interest of using the different products together.

Personality

Self Assessment :
TrustWillingness to compromiseReaction to stressProactivityCritical thinkingOptimismInterest in knowledgeIndependenceFlexibilityCuriosityCoordinationCollaborationAttention to detailAdaptabilityProblem solving

Knowledge

LinkedIn Assessment :
pharmacologyClinical trialsSAP R/3ICH-GCPMicrosoft OfficeProject CoordinationMicrosoft ExcelMetricsICFMedical writingGMPGood Laboratory Practice (GLP)PharmacokineticsAnalytical ChemistryBiostatisticsJMPin Vitro ToxicologyScientific WritingProject ManagementFormulation ChemistryCell Culture

Education

  • Clinet Project in Clinical Research from Cefochim in 2014
  • Master's degree in Pharmaceuticals Sciences from Université catholique de Louvain in 2013
  • Bachelor's degree in Pharmaceuticals Sciences from Facultés universitaires 'Notre-Dame de la Paix' in 2010
  • High School in Options : Sciences , Social Sciences and English from Sainte-Marie Huy in 2007

Training and Certification

  • Methods of Project Management in a multi-projects organization in 2015 Training
  • CLINET Project in 0000 Certification
  • Individual Dutch Immersion in 0000 Certification

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
English
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Work From Home:
    Yes, 0 to 1 days per week
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Belgique

Others

Driving License
  • Yes

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