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Clinical Study Specialist

Vor 7 Tagen


Zug, Zug, Schweiz TN Switzerland Vollzeit
Key Responsibilities
  • Advise Clients and Teams: Provide expert medical guidance to clients, project teams, sites, data safety monitoring boards, regulatory agencies, and third-party vendors.
  • Collaborate with Internal Departments: Work closely with internal departments to develop clinical development plans, protocols, and other essential documents.
  • Analyze Clinical Data: Review and analyze clinical data to ensure the safety of study participants.
  • Ensure Data Accuracy: Verify that reported data is accurate, complete, and verifiable, and that trial conduct adheres to approved protocols.

You will also address safety issues across the study from sites and the study team, review listings for coded events, and assist in Pharmacovigilance activities.