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Summary

as Freelance scientific/Medical Writer, i provide support for writing, peer review and Editing of scientific and clinical documents in the Pharmaceutical Industry. my expertise includes concept protocols, study protocols, science)" >Protocol posting, Informed Consent forms, study reports, Investigator brochures, standard operating procedures (sops), briefing documents, dcsis*, dsurs**, abstracts, and Publications. in addition, i provide Expert Training in writing of clinical study protocols and Clinical study reports.

*development core safety information, ** development safety update report

Experiences

Current Experience

  • Principal Medical Writer


    Since January 2015

  • Senior Medical Writer


    Since October 2013
    i execute a leading position in Medical Writer for various international Pharmaceutical companies. i provide Expert Training in writing clinical study protocols and Clinical study reports. I execute a leading position in medical writer for various international pharmaceutical companies. I provide expert training in writing clinical study protocols and clinical study reports.

  • Senior Medical Writer


    Since October 2013
    i execute a leading position in Medical Writer for various international Pharmaceutical companies. i provide Expert Training in writing clinical study protocols and Clinical study reports. I execute a leading position in medical writer for various international pharmaceutical companies. I provide expert training in writing clinical study protocols and clinical study reports.

  • Trainer


    Since January 2013
    Training in writing Laboratory reports and sops. Training in writing laboratory reports and SOPs.

  • Freelance Scientific Writer


    Since February 2007

  • Freelance Scientific Writer and founder of the company


    Since January 2007

Past Experience

  • Trainer

    May 2012 --- May 2014
    Training in writing of clinical study protocols and Clinical study reports.

  • Study Manager

    October 2013 --- January 2014
    post-Marketing trials with Medical Devices.

  • Scientific Writer

    January 2003 --- January 2007

  • Postdoctoral Researcher

    January 1999 --- January 2001

  • PhD Student

    January 1994 --- January 1998

Knowledge

LinkedIn Assessment :
ProtocolClinical researchPharmaceutical IndustryClinical Study DesignClinical trialsClinical DevelopmentGCPCROCTMSInformed ConsentICH-GCPoncologyInfectious diseasesCardiologyMedical writingPublicationsTrainingVaccinesCardiovascular DiseaseLifesciencesmolecular biologyImmunologyImmunofluorescenceCoachingClinical Data Management

Education

  • PhD in Biomedical and genetics from University of Leuven in 0000

Area / Region

Hoegaarden, België

Others

Driving License
  • Yes

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