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Jean-Louis MARQUES

Gosselies

En résumé

Entrepreneur, International Medical affairs, clinical trial operations professional and diagnostic specialist, with over fifteen years experience of research at site, CRO, and sponsor level, bringing a particular focus in driving innovation, projects and teams.

Leader by nature, combined with a high professionalism, I like to offer best customer experience and support people, team, to achieve their goals within agreed deadlines and budget.

I am a respected team worker, with essential inter-personal, communication, coaching end learner skills to be considered as a key interface with all CROs, vendors, health care processional (KOL,HCP, TL …) open to new opportunities for an innovative, ethical and patient care company.

Specialities :
- Complex problem solving orientation | Enthusiastic team member | Business acumen approach;
- Leadership of multidisciplinary teams within cross functional and international environment;
- Launch and commercialization activities support | Business strategy development;
- Start-Up Medical Imaging Core Labs | Lean Six Sigma – Green Belt | Professional Networking;
- KOL cultivation and management | Impactful delivery of scientific information to various medical audiences in English; French, Portuguese, and Spanish;
- Clinical trials management | Protocol review and implementation of all clinical trials (CT) phases |
Regulatory aspect of all CT phases, including ICH/GCP, development of SOPs;
- Clinical (CTs) experiences: neurology (dementia), bone diseases, oncology, cardiology, gastroenterology
& Cell Therapy - Autologous and Allogeneic programs;
- Multilingual: French - Portuguese - English - Spanish

Values: Trust | Integrity & Respect | Learning | Innovation | Teamwork | Entrepreneurial

Contact: jmarquestrindade@gmail.com
Mobile: +32 477 26 31 10

Mes compétences :
Leadership
Project manager
Business development
Clinical trials

Entreprises

  • Bone Therapeutics S.a. - Clinical Study Expert - Consultant freelance

    Gosselies 2018 - maintenant Medical & Clinical Advisor
    - Clinical Study Management
    - KOLs & HCPs engagement

    Area: Cells therapy (Autologous and Allogeneic products) | Multicentric and national/international studies
    Orthopaedic – bone Fractures (Non-union & delayed union)

    Achievements:
    • Retrospective study (Radiologcal union score development): Site selection - Study activation - Full CE approbation (Belgium, Germany) - Clinical operation strategy
    • Phase III (Bone Non Union): CRA lead - Site & activity close out
  • Marques Joao-Louiz - Entrepreneur | Senior Consultant Freelance

    2018 - maintenant Middle & Interim Management
    Medical Affairs - Imaging Diagnostic - Clinical trial Operation
  • Eli Lilly - Global Clinical Imaging Scientist

    neuilly sur seine 2017 - 2018 Focus: Global Medical affairs strategy | Alzheimer platform | Dementia diagnostic | KOL & HCP engagement | CIS Operation documentation lead management | Technical/Scientific/Medical support | Coach & learning program for internal and external stakeholders | Regional Clinical Imaging Scientist Operation | CIS = Medical Scientific Liaison associate | Customer services improvement (Lean Six Sigma)

    Area: Neurosciences & Alzheimer's Disease | PET/CT Biomarker | Amyloid PET Imaging tracer

    Achievements:
    • Successful launch support of PET Amyloid tracer in an international and cross-functional
    environment (SPAIN, CH,…)
    • Built strong relationship with the principal European KOLs, HCPs in Nuclear Medicine
    ensuring their engagement.
    • Significative Improvement of the customer services for product and service level complaints -
    Lean Six Sigma project
  • Eli Lilly - Regional Clinical Imaging Scientist

    neuilly sur seine 2013 - 2017 Focus: Act as liaison for though leaders and Health care professional to align interest, discuss biomarker use and Technical/medical information | Support on a non-promotional basis medical and scientific that support HCPs needs for the use of imaging (e.g; brain amyloid tracer) | Support clinical operation team, medical as marketing and sales team as well on their day-to-day activities related to Lilly PET Imaging agent (Amyvid) launch and development strategy objectives| Nuclear Medicine & diagnosis expert | Maintenance of scientific expertise, communication of scientific intelligence and clinical insight | Providing Technical Support to Imaging Health Care Professionals, set-up PET camera and imaging application related to PET imaging agent use | Support and facilitation of clinical and scientific research initiatives | Developing and delivering internal and external educational training (scientific and technical) | Serving as authors for publication, poster presentation | Providing recommendations to marketing for Scientific Experts and Imaging HCPs to serve as consultants, advisory board members, or speaker training faculty based on specific criteria

    Area: Neurosciences & Alzheimer's Disease | PET/CT Biomarker | Amyloid PET Imaging tracer

    Archievements:
    • Develop a culture of diagnostic vision at enterprise level | Cultivation of partner spirit
    between cross functional team end order to cash (O2C) team to improve customer
    satisfaction experience
  • Bone Therapeutics - Senior Clinical Officer

    2011 - 2013 Clinical Study Manager - Clinical Team Coordinator
    Management of the Clinical Department and all aspects of the clinical operations for assigned clinical trials to assure highest standards of clinical trial execution and Good Clinical Practice (ICH/GCP and EU Clinical Trial Directive).

    I manage, guide, direct the clinical trial team in order to ensure the smooth running of the clinical project and its delivery on time within a given budget.

    I supervise key study activities of strategies and regulatory documents, such as but not limited to IB, IMPD, briefing books, safety updates, DSUR, INDs, data management activity (eCRF, data entry and data base lock), site status (Feasibility and site recruitment, site initiation, patient recruitment, site monitoring), source document verification, Statistical Analysis and Clinical Study Report.

    I am responsible for providers selections (Request for proposal preparation, organize bid defense meetings, evaluate budget, manage budget negotiation and contracts).
  • Biomedical Systems - Project Manager

    2009 - 2011 Currently manage clinical research studies for an imaging core lab.

    Manage all aspects of the study which include; site initiation for hospitals/imaging departments all over the world;

    present at investigator meetings;

    prepare documents for FDA submission on behalf of the sponsor;

    manage flow of data to imaging core lab for processing;

    train radiologists for independent review regarding the study;

    manage all aspects of an independent review; process final data with quality control department and data management department for final submission to the sponsor.
  • Biomedical Systems - Medical Imaging Specialist

    2007 - 2009 Medical Imaging Specialist:

    Process all forms of data for research based clinical studies which involve imaging.

    Quality control and prepare all data received for importation into a database.

    Proficient using the following software; Adobe Premier, Adobe Photoshop, Digital Jacket, Isobuster, DicomWorks, Nuclear medicine application (Xeleris-GE), Microsoft Excel, Microsoft Word...

    Effectively communicate with various sites (hospital) regarding discrepancy issues with their data.
  • Cliniques Universitaire Saint Luc - Lead Nuclear Medicine Technologist (breath test)

    2001 - 2007 Gamma Camera,SPECT-CT, and PET-SCAN routine and researches activities in major Belgian university Nuclear Medicine department. Full responsibilities on Nuc med images acquisition, Images treatments and measurements. Veinipuncture certified. Clinical researches responsibilities.Image data quality control.

    Special and researches oriented procedures in SPECT, PET, CT: In vivo (scintigraphy, PETscan, breath test, injectable and radioactive substrate preparation).In vitro (ELISA, RIA, ECLIA, mass spectrometry).Leader Technologist of all Breath tests. Following-up patient, dosage samples, interpretation of the result, management material and products, quality control.Coordination of team, clinical study.Referent SIRILOG, Coordination computer links, security QC.

    Students mentoring from IPL, Brussels and European Erasmus Program mentorship in Nuc Med. Reader of IPL students thesis in medical imaging.

    President of the Society of technologists of the Belgian Society of Nuc Med
  • Cliniques Universitaire Saint Luc - Nuclear Medicine Technologist (breath test)

    2000 - 2007

Formations

  • Institut Paul Lambin - Universite Catholique De Louvain IPL (Bruxelles)

    Bruxelles 1995 - 1999 Biologie Medical

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