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Summary

looking for a challenging job with growth potential in biotechnological, Biomedical or Pharmaceutical sector. important personal values are: working in a team, lifelong learning and contributing to a better society.

Experiences

Current Experience

  • Clinical Trial Assistant (CTA)


    Since October 2014

    administrative and logistical support of cras in monitoring Hospital staff during a Clinical study. the main tasks are: Communication with Hospital staff, payments to physicians/patients and maintaining of the Clinical files.

    Administrative and logistical support of CRAs in monitoring hospital staff during a clinical study. The main tasks are: communication with hospital staff, payments to physicians/patients and maintaining of the clinical files.

Past Experience

  • Records Management Associate

    April 2014 --- September 2014

    controlling, completing and archiving of Clinical files according to ich-gcp guidelines. final purpose is to constitute a complete file in order to present it to the FDA for the approval of a new Medicine.

Personality

Self Assessment :
Analytical thinkingOrganizationProblem solvingCritical thinkingService orientedInterest in knowledgeAttention to detailFlexibilityReaction to stressIndependence

Knowledge

Self Assessment :
EnglishClinical trials Phase IClinical researchCTMSGood Clinical Practice (GCP)Quantitative PCR (qPCR)
LinkedIn Assessment :
ResearchCell CultureBiochemistryBioinformaticsRPCRICH-GCPmolecular biologyGeneticsBiotechnologyscienceCell biology

Skills and Expertise

Self Assessment :
Write papersAdministrative supportArchive study documentsCollaborate with medical team Interact with nurses Interact with physiciansManage Clinical Trial Management System (CTMS) Manage trial master file (TMF)Financial administrationInteract with pharmacistsDistribute trial suppliesEnsure good clinical practice (GCP)lifescienceSolve problems

Education

  • Master of Science (MSc) in Bioengineering sciences: cell and gene biotechnology from UGent in 2014
  • Bachelor of Science (BSc) in Bioengineering from Universiteit Antwerpen in 2011

Training and Certification

  • Introduction to ICH-GCP guidelines in 2014 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    Dutch
    Native
    English
    Professional Proficiency
    French
    Professional Proficiency

Work Preferences

  • Notice Period:
    3 weeks
  • Work From Home:
    Yes, 1 to 2 days per week
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Gent, België

Others

Driving License
  • Yes

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