POS 3253
Status 10

2x CRA Finland/Portugal

Beschreibung: For one of our Pharma clients we are seeking freelance support as: CRA Clinical Research Associate (M/F) home based in Portugal or Finland
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  • Assisting in initiating trial implementation including preparation of Ethics Committee/Institutional Review Board materials and communicating approval
  • Ensure clinical trials are conducted in a timely manner and in accordance with Standard Operating Procedures, the principles of ICH/Good Clinical Practice and all applicable regulations governing the conduct of clinical trials.
  • Managing, implementing and monitoring clinical studies in a team setting.
  • Verify that the rights and well-being of human subjects are protected and that the reported trial data are accurate, complete, and verifiable from source documents
  • Monitor responsibilities include: manage assigned clinical study protocols and amendments; track deviations; manage clinical trial sites and assure timely initiation and completion of clinical studies.
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  • Medical or science education
  • 1-2 years experience in clinical monitoring within the medical device or pharmaceutical industry
  • Knowledge of medical practice/techniques and terminology.
  • Knowledge of European regulations governing clinical trials.
Bemerkungen: WANTED: 2x CRA Finland/Portugal (M/F/D). Please contact +49 89 18 90 998 40 or Skills: CRA (Clinical Research Associate), English, Finnish, Neurology, Portuguese, Psychiatry
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Interesse geweckt?
Auf geht's!
Beginn: Asap
Laufzeit: 2 years
Einsatzort: Portugal & Finland
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