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• Gesucht: Clinical Research Associate in Basel (dreisprachig Deutsch, Englisch und Französich)

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  Lucie Labide

  The company name is only visible to registered members.

  Gesucht: Clinical Research Associate in Basel (dreisprachig Deutsch, Englisch und Französich)

  We are currently looking for a CRA who is accountable for site relationships with the following responsibilities:
  " Facilitate preparation and collection of site level documents.
  " Perform monitoring visits according to monitoring plan.
  " Manage site drug supply management.
  " Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc.).
  " Assure continual GCP, ICH and client SOP compliance (Informed consent process, Source data verification, AE and SAE reporting, IN
  protocol, drug accountability etc.).
  " Author study monitoring reports.
  " Perform data query resolution process (both at Site and with Data Management).
  " Execute site closeout activities.
  
  You will monitor several protocols across various therapeutic areas. Sponsor works in all areas except oncology. Some of the main indications include: CNS Multiple Sclerosis , Cardiovascular Heart failure, Respiratory COPD, transplant
  
  PROFESSIONAL REQUIREMENT:
  " Desired 2 years experience in clinical research
  
  " Knowledge and experience in international standards (GCP/ICH), international (FDA, EMEA) and local regulations.
  " Expertise in communication, managing multiple priorities and computer literacy
  
  " Proficiency in English, German and French.
  
  
  If you would like to apply for this position, please send me your CV and contact details at llabide@rpsweb.com.
  
  • 22 Sep 2011, 09:59 am
  Lucie Labide wrote: > We are currently looking for a CRA who is accountable for site > relationships with the following responsibilities: > " Facilitate preparation and collection of site level documents. > " Perform monitoring visits according to monitoring plan. > " Manage site drug supply management. > " Ensure site activities in line with milestones (i.e. startup, > recruitment, closeout, etc.). > " Assure continual GCP, ICH and client SOP compliance (Informed > consent process, Source data verification, AE and SAE reporting, IN > protocol, drug accountability etc.). > " Author study monitoring reports. > " Perform data query resolution process (both at Site and with Data > Management). > " Execute site closeout activities. > > You will monitor several protocols across various therapeutic areas. > Sponsor works in all areas except oncology. Some of the main > indications include: CNS Multiple Sclerosis , Cardiovascular Heart > failure, Respiratory COPD, transplant > > PROFESSIONAL REQUIREMENT: > " Desired 2 years experience in clinical research > > " Knowledge and experience in international standards (GCP/ICH), > international (FDA, EMEA) and local regulations. > " Expertise in communication, managing multiple priorities and > computer literacy > > " Proficiency in English, German and French. > > > If you would like to apply for this position, please send me your CV > and contact details at llabide@rpsweb.com.