Clinical Research Associate

vor 1 Monat


Home Office, Schweiz IQVIA Vollzeit

We are currently hiring a **CRA (M/F/d) **to work in our multi-sponsor department and to join our team in a home-based position in Switzerland.

Beside establishing strong relationships with our clients and the involved investigators, you will conduct monitoring on complex clinical trials and assure the adherence to good clinical practices, standard operating procedures, and study protocols.

**While projects vary, your typical responsibilities might include**:

- Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
- Establishing regular lines of communication plus administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Conducting remote monitoring

**You should have**:

- A Bachelor's or higher level degree in a health care or other scientific discipline or educational equivalent
- At least **one year of on-site monitoring experience**
- Alternatively, you should have an equivalent combination of education, training and experience in the field of clinical trials
- Fluency in **German and Italian** are required, as well as **English**. Additional communication skills in French are a plus
- You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements
- Flexibility to travel



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