Alexander Parmentier

Experience

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  IKWV - Intercommunale Kustreddingsdienst West-Vlaanderen

  Jul 2010 - Oct 2015

  Lifeguard
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  UZ Gent

  Jul 2014 - Jun 2015

  Undergraduate Student Researcher

  Masterthesis:Cell-cell communication in the neuro-glio-vascular unit during inflammationExperiences: o Literature studyo Writing protocols for the use of laboratory equipmento Prepare, work out, report and analyse testsSkills: Cell work, PCR, Western Blotting, zymography, immunohistochemistry, SLDT

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  Skikot

  Dec 2015 - May 2016

  Destination manager

  o organising weekly arrivals and departures of clients and groups o weekly preparing skikot delivery and working close together with local government o fixing problems for clients and making their trip as pleasant as possibleo keeping care of a cashbook and administrationo sustain contact with accommodations, skipass office, bars, restaurants, ski school, rental shopso promoting and representing the brand skikot in the villageo organising a full animation program for all the skikot clientso sustaining contact and briefing the main skikot bureau in Belgium with an weekly reporto manage a team of skikot guides Show less

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  EORTC

  Feb 2017 - Jan 2020

  EORTCThe European Organisation for Research and Treatment of Cancer (EORTC), based in Brussels, Belgium, brings together European cancer clinical research experts from all disciplines for trans-national collaboration. The EORTC Network comprises more than 5500 collaborators from all disciplines involved in cancer treatment and research in more than 930 hospitals and institutions in 27 countries. Through translational and clinical research, the EORTC offers an integrated approach to cancer treatment and medical practices.CRAo Travel 60% of working time across European countries (BE, NL, FR, GB, AT, ES, IT, PL, SI, .. )o Perform on-site monitoring visits to EORTC participating institutions according to the monitoring plan and following the EORTC SOPs and ICH-GCP guidelineso Ensures and control site compliance with study protocol and regulatory obligationso Address issues in a manner that is beneficial for the site and the EORTC teamo Report the findings of the on-site monitoring visits according to EORTC standardso Follow up the site findings until resolution with the support of the EORTC study team and Quality Assurance and Control Unito Perform site training whenever needed during the study conducto Ensure close collaboration between all actors of clinical trial research, as a privilege link between investigational sites and the EORTC study teamo Contributes in the on-site training program of Junior CRAs--> Phase II Lung Onco trials (Merck and AstraZeneca) Show less o Travel min 40% of working time across European countrieso Perform on-site monitoring visits to EORTC participating institutions according to the monitoring plan and following the EORTC SOPs and ICH-GCP guidelineso Ensures and control site compliance with study protocol and regulatory obligationso Address issues in a manner that is beneficial for the site and the EORTC teamo Report the findings of the on-site monitoring visits according to EORTC standardso Follow up the site findings until resolution with the support of the EORTC study team and Quality Assurance and Control Unito Perform site training whenever needed during the study conducto Ensure close collaboration between all actors of clinical trial research, as a privilege link between investigational sites and the EORTC study team--> Phase II Lung Onco trials (Merck and AstraZeneca) Show less

  • Clinical Research Associate

    Jan 2019 - Jan 2020

  • Junior Clinical Research Associate

    Apr 2018 - Dec 2018

  • Clinical Data Manager

    Feb 2017 - Mar 2018
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  ICON plc

  Jan 2020 - Dec 2024

  Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH-GCP guidelines.Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sitesReviews and verifies accuracy of clinical trial data collected, either onsite or remotelyProvides regular site status information to team members, trial management, and updates trial management toolsCompletes monitoring activity documents as required by PRA SOPs or other contractual obligationsWorks closely with other clinical team members to facilitate timely resolution of trial and/or clinical issuesEscalates site and trial related issues per PRA SOPs, until identified issues are resolved or closedPerforms essential document site file reconciliationPerforms source document verification and query resolutionAssesses IP accountability, dispensation, and compliance at the investigative sitesVerifies Serious Adverse Event (SAE) reporting according to trial specifications and ICH-GCP guidelinesCommunicates with investigative sitesUpdate applicable tracking systemsEnsures all required training is completed and documentedServes as observation visit leaderFacilitates audits and audit resolutionMentors junior level CRAs and serves as a resource for new employeesServes as observation and performance visit leaderMay be assigned additional Clinical operation tasksMay serve as a resource for and interact with other functional areas to resolve site issues and facilitate trial timelinesMay be assigned clinical tasks where advanced negotiating skills are required Show less

  • Senior CRA, outsourced to Bayer

    Sept 2022 - Dec 2024

  • CRA II, outsourced to Bayer

    Jan 2020 - Sept 2022
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  Imec

  Jan 2025 - now

  Intern