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Experiences

Current Experience

  • Medical Affairs Trainee Belgium
    Since November 2014

    Development of Protocols

    Management of EMAEI Portfolio

    Development of New Study Ideas

    Medical Affairs

    Medical Writing

  • Thesis Student
    Since September 2013
    Exploratory phase I clinical trails for development of target engagement TRP channel biomarkers. At the Center of clinical pharmacology unit, UZ Leuven. Under the guidance of Prof. Dr. Jan de Hoon

Past Experience

  • Intern
    January 2013 --- May 2013
    Research lab rotation internships at the Laboratory of Neuroscience and neurodegenerative disorders, Laboratory of experimental endocrinology and laboratory of toxicology

  • Voluntary Internship
    July 2011 --- August 2011
    Procurement and dispensing of prescriptions

  • Trainee
    February 2011 --- February 2011
    Trainee ship in Production, Quality Control, and Packaging of sterile and non sterile pharmaceuticals.

Personality

BrightOwl Assessment :
IndependenceSelf-disciplineEfficiencyOrganizationStrivingKindnessAuthenticityInterest in knowledgeCuriosityPerspectiveApproachabilityDiligence

Knowledge

BrightOwl Assessment :
BiomarkersClinical researchLaboratoryClinical trial designPhase IMicroneedle technology Biostatistics
Self Assessment :
Clinical operationsEnglishBiomarkersPhase IEthics submission and approval processClinical trial designICH GCP guidelinesClinical Data Management (CDM)Clinical researchMedical writing Medical devicesMedical affairsEMEAIMedical Journalism Medical Journalism
LinkedIn Assessment :
Clinical researchStatisticsPharmaceutical SciencesGCPPharmaceutical Industry

Skills and Expertise

BrightOwl Assessment :
Use western blotting techniqueUse laser doppling imaging technique Develop protocols Interpret dataWrite combined statistical and medical reportsCreate SOPsAct as the main line of communication between the sponsor and the investigator Use a confocal microscopy
Self Assessment :
Write combined statistical and medical reportsCreate Standard Operating Procedures for each study or clinical trial.Act as the main line of communication between the sponsor and the investigatorDevelop protocolsInterpret dataBiomarker ResearchMedical Affairsscientific writingMedical JournalismEMEAIDevelop ICH/GCP compliant processes

Education

  • Master of Science in Biomedical Sciences, Major in Research in Clinical Research, Early Phase Trials. from Katholieke Universitiet Leuven in 2014
  • Bachelor's Degree in Pharmaceutical Sciences from University of Kashmir in 2011

Training and Certification

  • ICH and GCP Guidelines (Phase I) in 2013 Training
  • CRP in 2013 Certification

Work Preferences

  • Work From Home:
    No
  • Work Regime:
    Permanent position
    BrightOwl freelancer
    BrightOwl employee
  • International:
    Yes

Area / Region

Leuven

Others

Driving License
  • No