Pharma / Medical

On behalf of our esteemed customer based in Mendrisio area, we are looking for the following profile:


Main responsibilities and activities:

  • Responsible to develop, coordinate and implement research and administrative strategies essential to the successful management of the clinical trials and clinical investigations;
  • Perform a variety of duties involved in the organization, documentation and compilation of clinical research data.
  • Coordinate Sponsor, monitors, laboratories, subcontracted services and Investigators.
  • Provide support and/or prepare study protocols, clinical investigation plans and other specific study docu ments; write/check subject's/patient's information sheet/informed consent and organise their translations.
  • Responsible for submission of study documents to relevant stakeholders for approval or /notification, and perform actions needed to obtain study authorisation.
  • Responsible to collect, review, process and report trials deviations


  • Degree in Pharmacy/Life Science
  • 5-10 years of relevant Experience in a CRO environment
  • Experience on phase 2-3 of Clinical studies
  • Fluent english mandatory

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