Clinical Research Associate (CRA) Job at SOCAR Research in Nyon, VD

Job Description

Your role:
You will be part of a young and dynamic multidisciplinary project research team. Part of your responsibilities will be to perform both site management activities (remotely and onsite) in addition to clinical monitoring of designated projects in accordance with applicable SOPs and regulations. This will involve travelling to clinical sites located mainly in Europe to perform source data verification in addition to other specific, site-related activities. The remainder of the time will be office-based and spent performing multiple and varied tasks in data management such as checking clinical data for completeness and medical consistency, in preparation for statistical analysis.

minimum required educational qualifications

Bachelor’s degree (biological science, nursing, physiotherapy, pharmacy or any health related discipline)

In lieu of a degree, a minimum of two years of directly related full-time experience, such as Site Study Coordinator

preferred skills / attributes


Rigorous attention to detail

Strong regulatory knowledge including ICH GCP

Clinical research experience

Excellent interpersonal, verbal and written communication skills

Sound problem-solving skills

Ability to prioritise multiple tasks and achieve project timelines

Ablility to travel a minimum of 35% (average); be in possession of a valid driving licence


Fluent in English (oral and written)

Excellent command of German

Another European language would be an advantage

About Company

Company: SOCAR Research

Company Location:  Nyon, VD

About SOCAR Research