Sponsor Dedicated DACH Clinical Research Associate based in Germany (m/f/d)

• Identify and assess new potential investigators and sites.
• Recommend sites during feasibility and selection phases.
• Conduct pre-study, initiation, monitoring, and close-out visits.
• Monitor site performance, data quality, and protocol compliance.
• Act as a key point of contact for site personnel, providing training and support.
• Use data insights to assess risks and drive decisions.
• Support regulatory audits, EC submissions, and system access coordination.

• University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
• Basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations governing clinical trials.
• Solid understanding of clinical research processes, regulations, and methodology .
• Strong organizational and time management skills.
• Ability to build and maintain relationships
• 1 to 3 years of monitoring experience required within CRO or Pharma environment.

Why Join Us?

• Be part of a sponsor-dedicated team with a strong pipeline and purpose.
• Enjoy regional monitoring—minimizing travel while maximizing your impact.
• Collaborate with passionate professionals in a supportive environment.
• Contribute to meaningful research that improves lives.

Learn more about our EEO & Accommodations request here .