freelance clinical research associate ( cra ) germany – medical devices

• 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 as full partners. We take care of a large part of the administrative burden so you can focus on the content of your work.

• You can count on timely and correct payment of your invoices (30 days).
• As a freelancer, you also have an account manager as your dedicated point of contact and are welcome at our events to stay connected with the community.
• Thanks to our extensive client network, we proactively look for your next assignment even before your current project ends.