You will:

• Conduct and report all types of onsite monitoring visits as well as remote visits
• Perform CRF review, source document verification and query resolution
• Maintain accurate trial documentation, and help ensure participant safety, data integrity and compliance with study protocols and regulatory requirements
• Be responsible for site communication and management
• Build effective relationships with investigators and study teams
• Be involved in site identification process

Qualifications

• Completed advanced CRA/Clinical Monitoring training (e.g., mibeg, Pharmaakademie, or comparable)
• University degree in life sciences, natural sciences, pharmacy, medicine, or another relevant scientific/healthcare field
• Demonstrated knowledge and understanding of Good Clinical Practice and clinical trial processes
• Prior experience in clinical research is preferrable
• Strong communication and organizational skills
• Attention to detail and willingness to take accountability
• Ability to manage several priorities and learn quickly
• Very good German and English language skills
• Willingness to travel to investigational sites within Germany