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Medical Monitoring Specialist

vor 1 Woche


Zürich, Zürich, Schweiz Syneos Health Vollzeit

**Job Summary**

The Clinical Research Associate will perform monitoring and site management activities for Phase I-IV clinical research projects to assess the progress of clinical projects at assigned investigative/physician sites.

**Key Responsibilities**

  1. Perform site qualification, site initiation, interim monitoring, site management activities and close-out visits to ensure protocol compliance.
  2. Verify the process of obtaining informed consent and demonstrate diligence in protecting the confidentiality of each subject/patient.
  3. Assess site processes, conduct source document review, and verify required clinical data entered in the case report form (CRF) is accurate and complete.

**Qualifications**

  • Min. Bachelor's degree in Life Sciences or equivalent combination of education, training, and experience.
  • Fluency in English, German, and French, with Italian as an additional advantage.
  • Previous years of monitoring experience in Switzerland and experience with submissions (EC and Swissmedic).

**About Us**

We are a fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success.