Description

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.

Requirements

• •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

Tasks

• •Perform site selection and initiation visits
• •Conduct monitoring and close-out visits
• •Support the development of subject recruitment plans
• •Evaluate site practices for quality and regulatory compliance
• •Track regulatory submissions and recruitment progress
• •Ensure case report form (CRF) completion and resolve data queries
• •Collaborate with study site experts and client representatives
• •Engage in remote monitoring and study start-up processes as needed
• •Mentor less experienced team members and provide subject matter expertise

Benefits