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Summary

Please see my website: http://www.lunamedicaconsulting.com/

Experiences

Current Experience

  • Editor and Reviewer
    Since April 2013
    Reviewer, proof-reader, editor and translator of pharmaceutical documents from all stages of drug development.

Past Experience

  • Disclosures Specialist
    November 2013 --- May 2014

  • Freelance Medical Writer
    July 2013 --- October 2013
    Write up of a CSR, updating a protocol.

  • Safety scientist/Regulatory Writer
    November 2011 --- June 2012
    Writing of periodic safety update reports (PSURs), Periodic Adverse Drug Experience Reports (PADERs), Development Safety Update Reports (DSURs) Annual Periodic Reports (APRs), Medical Safety Assessments (MSAs), and Toxicity Reports.

  • Advanced Clinical Coordinator - Critical Care Cardiology
    March 2011 --- July 2011

  • Pharmacovigilance expert
    January 2010 --- December 2010

  • Medical Writer/Drug Safety Scientist
    January 2008 --- January 2010

  • Postdoctoral Fellow
    January 2005 --- January 2008

Knowledge

LinkedIn Assessment :
Clinical trialsPharmacovigilanceMedical writingPharmaceutical IndustryClinical DevelopmentGCPRegulatory affairsRegulatory submissionsCTMSCROICH-GCPClinical researchMedDRAMedical DevicesLifesciencesMedical affairsoncologyLife Sciences

Education

  • in from Universidad Autónoma de Baja California in 0
  • in from Université de la Sorbonne, Paris, France. in 0
  • PhD in Medical Science from The Australian National University in 0

Area / Region

Gex, France

Others

Driving License
  • No