Clinical Research Associate

Proclinical has partnered with a global Contract Research Organisation in search for Clinical Research Associate. The role will be home-based in Switzerland , and is an opportunity to propel your clinical career at an established company.

Job Responsibilities

• Monitoring independently different sites, including RBM.
• Participation in investigator meeting as necessary
• Ensuring the trial is conducted in accordance with the approved protocol ICH-GCP guidelines, SOPs etc
• Ensuring effective communication between investigational sites and internal/external stakeholders
• Working on project work and initiatives for process improvement as required

Skills and Requirements

• Degree in pharmacy, life science or related field
• Experience in a pharmaceutical, biotech or CRO company
• Independent clinical monitoring experience
• Fluency in English, German and French ideally (English and 1 of the two other languages will be accepted)
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Excellent understanding and demonstrated application of GCPs and applicable SOPs
• Management of regulatory and / or IEC questions
• Development and preparation of the local informed consent form
• Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
• Proven flexibility and adaptability
• Ability to work in a team or independently as required

To Apply

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

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