Description

In this role, you will manage clinical trials by selecting sites, monitoring progress, and ensuring compliance with regulations. You will work closely with study teams and investigators, contributing to the development of innovative medicines.

Requirements

• •University degree in life science, scientific discipline, or apprenticeship in health care
• •Minimum of two years of on-site monitoring experience
• •Knowledge of clinical research regulatory requirements, GCP, and ICH guidelines
• •Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
• •Good command of German and English
• •Flexibility for business travel up to 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 integrity
• •Ensure compliance with GCP and ICH guidelines
• •Track regulatory submissions and recruitment progress
• •Complete case report forms and resolve data queries
• •Collaborate with study site experts and client representatives

Benefits