566 days ago on apr.ch


APR Applied Pharma Research SA

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 Please refer to JobSuchmaschine in your application


  • to coordinate clinical activities associated with study start-up and management in Europe and, if required, worldwide, by working closely with the Head of the Clinical Affairs;
  • to support the preparation & review of relevant study documents including synopsis/protocol, subject information & informed consent form, study guidelines, monitoring plans, investigator brochures, CRFs, and clinical study reports;
  • to maintain study timelines and monitor study progression/budget;
  • to get involved in co-monitoring activities, when required;
  • to contribute to the review of data listings;
  • to contribute to or coordinate the preparation and conduct of investigators’ meetings;
  • to coordinate study-level investigational product arrangements, accountability and reconciliation; participate in and support investigational study teams, if required, or CRO teams;
  • to participate in the selection of CROs/vendors, and work closely and effectively with them;
  • to provide input for screening and enrolment progress, and identify barriers to screening and enrolment and provide solutions;
  • to establish solid and professional relationships with existing partners (licensees) and KOLs;
  • to continue to increase knowledge of clinical research, clinical operations, and relevant therapeutic areas.