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 collaborate with experts, ensure compliance with regulations, and support recruitment efforts, all while enjoying opportunities for professional growth.

Requirements

• •University degree in life science or other scientific discipline or apprenticeship in health care field
• •Minimum of two to four years of on-site monitoring experience or equivalent combination of education, training, and experience
• •Knowledge of clinical research regulatory requirements, i.e., GCP and ICH guidelines
• •Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
• •Fluency in German at C1 level and good command of English
• •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 data query resolution
• •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