Cra, Switzerland

Proclinical are recruiting for a CRA, Switzerland to join a CRO. This role is on a permanent basis with the ability to work remotely from anywhere in Switzerland.

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**Responsibilities**:

- Handle processes and regulations from various sponsors and/or supervision settings.
- Enable efficient communication between investigative sites, the client organisation and the company's project team through written, oral, and/or electronic contracts.
- Conduct and arrange all features of the clinical monitoring procedure.
- Perform supervision actions on an independent basis.
- You will perform either remote or on-site visits to examine protocol and regulatory compliance as well as handle necessary documentation.
- Other duties may be assigned.

**Key Skills and Requirements**:

- Educated to a degree level in a life science discipline or obtained a registered nursing certification or corresponding and pertinent formal academic/vocational training.
- Acquaintance with on-site supervision on an independent basis within a pharmaceutical or clinical research organisation.
- Comprehension of ICH-GCP, EU and FDA needs.
- Comprehension of medical/therapeutic area expertise and medical vocabulary.
- Works well with others.
- An organised individual with the ability to manage time efficiently.
- Communication skills both verbally and in writing.
- Fluency in the English language with knowledge in German or French would be ideal or any other languages at a C1 level or Italian at a B1 level would be ideal.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

LI-LS3

CRODelivery

Clinical