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SOTIO is a biotechnology company developing a next generation Active Cellular Immunotherapy based on activated dendritic cells for the treatment of cancer and autoimmune diseases. SOTIO continues to develop new therapies to address unmet medical needs using its immunotherapy platform and proprietary cell-based technologies


Current Experience

  • MSLs Manager
    Since October 2015

Past Experience

  • Medical Sciences Lead Europe / Oncology ( Prostate, NSCLC and Ovarian )
    August 2014 --- July 2015

  • Manager Medical Sciences - Ophtalmology / France
    October 2012 --- July 2014

  • Medical Sciences Liaison / Oncology & Critical Care
    June 2010 --- September 2012
    ➢ Responsible for the field-based provision of expert clinical and scientific information to customers. ➢ Responsible for the management of collaborative relationships with key opinion leaders, thought leaders and health care ➢ Providing support to the national business unit to provide clinical insight; technical expertise and scientific training to staff.

  • Clinical Trial Managements positions / CRA, SCRA, CTM, CPM and Clin Ops Manager
    February 2004 --- May 2010
    ➢ Projects / Line management ( depending on the project and the client) ➢ Different Phases: Phase I, phase II, phase III and PMS ➢ Different therapeutic areas: Oncology (Colorectal, Prostate, Liver and NSCLC), Ophthalmology, Respiratory, Onco-hematology Nephrology, ICU and Hepatitis. ➢ Different clients (Allergan, Cougar, Gilead, LFB, Roche, Anosys, BMS, Eyetech, Myogen and Otsuka)

  • Clinical Trials Study Coordinator
    May 1998 --- December 2003
    ➢ Facilitate the conduct of clinical trials ➢ Responsable for coordination, collection and delivery of research data and pertinent information. ➢ Assist with the implementation of QA tools and the conduct of QA audit as needed ➢ Assist with training and mentoring new staff.

  • EMEA Pharmacovigilance Specialist
    April 1997 --- April 1998
    ➢ Collect and process incoming adverse event reports from all sources ➢ Perform initial assessment of seriousness, expectedness, causality, and reportability ➢ Complete and QC data entry of incoming reports ➢ Identify missing or discrepant information and perform active follow-up ➢ Prepare expedited reports for submission to regulatory authorities and ethics committees ➢ Serve as pharmacovigilance resource to Clinical Development Teams


LinkedIn Assessment :
oncologyMedical DevicesClinical researchBiotechnologyClinical trialsClinical DevelopmentPharmacovigilanceCTMSCROMedical affairsTherapeutic AreasICH-GCPDiabetesGCPGastroenterologyDermatologyRegulatory affairsHematologyRegulatory submissionsClinical Study DesignEDCPharmaceutical IndustryClinical Data ManagementNeurologyEndocrinologyClinical monitoringSOPInfectious diseasesMedical writingCardiologyDrug DevelopmentImmunologyLifesciencesPharmaceuticsOphthalmologyLife Sciences


  • in from Master Immunology and Biotherapy in 2015
  • in from Master in Oncology pharmacology in 2012
  • in from Master of International Business (MIB) in 2002
  • in from Master in Pharmacology & Safety in 1998
  • in from Certificate of Statistical Studies Applied to Medicine (CESAM) in 1997
  • in from Diploma Training of Clinical Trials Investigators (FIEC) in 1996
  • in from Pharm.D in 1991

Area / Region

Paris, France


Driving License
  • No