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Welcome to my Linkedin profile! Currently working at Sanofi Pasteur as a Clinical Trial Manager, I am involved in several clinical studies across Asia. I am looking for my next challenge, starting November 2016 (worldwide mobility). Please have a look at my profile and feel free to contact me!


Current Experience

  • Regional Clinical Trial Manager - VIE Philippines Makati, NCR, Philippines
    Since November 2014

    R&D department

    • Responsible for ensuring that clinical and epidemiological research studies are conducted at quality, high performing sites in accordance with applicable regulations, ICH GCP guidelines and Sanofi Pasteur SOPs - Identification, selection and set-up of study sites
    • Selection of CROs (monitoring) - IEC/IRB submissions and Health Authorities submissions
    • Creation of study documents: operating guidelines, CRF completion guidelines, monitoring plan
    • Review of study documents: protocol, ICFs and Assent forms, diary cards, CRF, data monitoring plan and Clinical Study Report
    • CRAs training, Follow up of the monitoring activity done by CRAs and conduct of quality control visits on site
    • Participate in the preparation and conduct of investigator meetings
    • Responsible for the vaccines supplies and vaccine returns/destruction as well as the management of biological samples
    • Ensure Trial Master File (TMF) updates & QC
    • Participate as the study management representative in the clinical team: ensure appropriate communication of status updates and issues regarding site management and monitoring
    • IMPACT Polaris Super User Asia Pacific (CTMS): monthly training of newcomers and daily support to the Asia Pacific team


    • Clinical study (phase IV) on flu vaccine in the Philippines (annual flu vaccine)
    • Epidemiological study on dengue in India (pediatric and adult population, 14.000 subjects)
    • Pharmacoepidemiological studies on dengue in Philippines and Malaysia (pediatric and adult population, 5.000 subjects)

Past Experience

  • Clinical Project Manager Trainee Lyon, France
    October 2013 --- September 2014

    Global Medical Affairs / Chief Medical Office department (GMA - CMO PPO)

    • Responsable for ensuring that clinical trials and epidemiological studies are executed in line with Sanofi Pasteur strategy in terms of planning, budget and quality, and according to local and international regulations
    • Determining strategic and operational feasibility of the study
    • Coordination of information on study performance from all team members: monitoring, logistics, data-management, biostatistics, medical writing, supply chain...
    • Planning of the trial (timelines, budget): creation and updating of Gantt charts (OPX2)
    • Contribution to the identification and selection of potential sites and CROs
    • Development and justification of AEDs - Planning, negotiation and follow-up of the costs of the studies (investigator fees, outsourcing, logistics)
    • Development of study agreements in collaboration with legal department
    • Follow-up of investigators and CROs invoicing
    • Participation in the development of protocols, ICFs and assents, clinical study reports
    • Planning and order of vaccine doses (CSC Order Management)
    • Management of TMF documents


    • Clinical trial (phase IV) on Japanese encephalitis vaccine in Thailand (10 centers, 10.000 subjects)
    • Flu studies (phase III and IV) in Taiwan, France and Belgium
    • Epidemiological studies in Kenya, Ivory Coast and Cameroun

  • Methodologist - Pharmacy internship Poitiers, France
    August 2013 --- September 2013

    • Regulatory submissions to French Health Authorities and Ethics Committees (ANSM, CPP)
    • Help in study design, protocol writing

  • Clinical Research Associate (CRA) - Pharmacy internship Poitiers, France
    June 2013 --- July 2013

    • Intensive Care Unit: Observational studies

  • Biostatistician - Internship
    May 2013 --- May 2013
    Statistical analysis of the data from a clinical study on hypertension and diabetes using the StatView software.

  • Clinical Pharmacist - Pharmacy internship
    April 2013 --- April 2013
    - Cardiology/Intensive care: Medical device - Medicinal products derived from human blood or human plasma, Hospital Pharmacy: SOPs

  • Clinical Research Associate (CRA) in Oncology - Internship Paris, France
    December 2012 --- March 2013

    • Clinical trials setting up, patients screening and monitoring, follow up with the patients
    • Biological samples processing (PK-PD)
    • CRF and eCRF filling, adverse events recording, monitoring visit, queries solving


LinkedIn Assessment :
BiotechnologyClinical DevelopmentClinical monitoringClinical researchClinical trialsCTMSGCPICH guidelinesLearning AgilityoncologyPharmaceutical IndustryPharmacyProject ManagementVaccines


  • Doctor of Pharmacy (PharmD) in Clinical Trials from University of Poitiers in 2014
  • MSc, European Diploma in Pharmaceutical Medicine (EUDIPHARM) in Institut de Pharmacie Industrielle de Lyon (IPIL) from Université Claude Bernard Lyon 1 in 2014
  • College of Pharmacy in from Oregon State University in 2012

Training and Certification

  • Certificate in Essential GCP Certification
  • Vaccinology Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency

Work Preferences

  • Work From Home:
  • International:

Area / Region

Makati, NCR, Philippines


Driving License
  • Yes