Clinical Research Associate or SrCRA(m/w/x)

In this role, you will be actively involved in the clinical research process, from site selection to monitoring and close-out visits. You will ensure compliance with regulatory standards while collaborating with experts and mentoring team members, all from the comfort of your home in Switzerland.

Anforderungen

• •University degree in life science or other scientific discipline or apprenticeship in health care field
• •Minimum of two years of on-site monitoring experience or equivalent combination of education, training, and experience
• •Knowledge of clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• •Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
• •Fluent verbal and written language skills in German and English (C1 level) plus good verbal demand in French and Italian
• •Flexibility to travel up to 40-60% of working time
• •Driver’s license class B