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.

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.

If you are having difficulty in applying or if you have any questions, please contact Leonie Schluter at +44 203 100 0951.

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.

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