Clinical Research Associate 2 or Senior Clinical Research Associate 1 (m/w/d), Single Sponsor

In this home-based role within IQVIA's single sponsor department in Germany, you drive clinical trial delivery across sites, from initiation to close-out. You support recruitment strategy and ensure GCP/ICH compliance while coordinating with sites and client representatives. You may participate in remote monitoring and study start-up activities, while mentoring junior staff. This position offers growth, world-class training, and a path to broaden therapeutic experience.

• permanent employment contract
• home-office and flexible working schedules
• competitive salary
• company car or car allowance
• accident insurance
• pension

• Perform site selection, initiation, monitoring and close-out visits
• Support the development of a subject recruitment plan
• Evaluate site practices for quality and regulatory compliance (GCP/ICH)
• Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data queries
• Collaborate with study sites and client representatives
• Possibility of remote-monitoring, study start-up involvement, and therapeutic area specialization
• Mentor less experienced team members and serve as a subject matter expert on topics

• University Degree in life science or other scientific discipline
• 2–4 years of on-site monitoring experience or equivalent
• Knowledge of GCP and ICH guidelines
• Strong written and verbal communication, attention to detail, ability to work in a fast-paced environment
• Fluency in German (C1) and good command of English
• Flexibility to travel 40–60% of working time
• Driver’s license class B

• strong communication skills
• attention to detail
• ability to work in fast-paced environment
• Good Clinical Practice (GCP)
• International Conference on Harmonization (ICH) guidelines
• site monitoring