clinial research associate - duitsland

• Comprehensive site management: oversee and manage investigator sites, maintaining clear and proactive communication with site staff and the sponsor.
• Full-cycle monitoring visits: independently conduct and manage all key monitoring visit types, including Site Initiation Visits, Interim Monitoring Visits, and Close-out Visits.
• Regional Travel & On-Site Presence: Execute required on-site monitoring activities and hospital visits, which are primarily situated across central, northern, and western Germany.
• Compliance & training: actively participate in sponsor training and ensure all clinical trial activities strictly adhere to protocols, regulatory guidelines, and quality standards.
• Reporting: deliver clear, ad-hoc, and scheduled updates via email, telephone calls, and meetings to Clinical Trial Leaders.

• Experience: minimum of 5 years of clinical monitoring experience, with a proven track record of handling the main monitoring visit types (Site Qualification, Site Initiation, Interim Monitoring, and Close-Out).
• Education: minimum of a Bachelor’s degree within a Life Science field.
• Industry expertise: previous experience monitoring medical device studies is highly preferred.

At Randstad Professional, we consider our freelancers to be full partners. We take away much of the administrative burden so you can focus entirely on your work.

• You can rely on timely and accurate payment of your invoices (30 days).
• As a freelancer, you also have a dedicated account manager as your main contact person and are welcome to attend our events to stay connected with the community.
• Thanks to our extensive client network, we proactively search for your next challenge before your current project comes to an end.