Sponsor Dedicated DACH Clinical Research Associate based in Germany

Fortrea; München; On-site; EUR 52,000 - 68,000; Full time

Job summary

Fortrea is seeking a Clinical Research Associate (CRA) to monitor sites in Germany, Austria, and Switzerland. You will oversee pre-study to close-out visits, ensure protocol compliance, and train site staff. The role emphasizes data-driven risk assessment and close collaboration with sponsors to advance healthcare research.

Qualifications

• 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

Responsibilities

• 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

Skills

Site monitoring

GCP/ICH knowledge

Project coordination

Regulatory coordination

Education

Life sciences degree

Tools

EDC systems

Regulatory systems

Job description

Make a meaningful impact in clinical research by joining our sponsor-dedicated team as a Clinical Research Associate (CRA) . This role offers the opportunity to monitor sites in Austria and in Switzerland , while working on cutting-edge studies that shape the future of healthcare.Key Responsibilities: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.Required Qualifications :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 relationships1 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.We invite qualified candidates who are committed to excellence in clinical research to apply and become part of Fortrea’s mission to advance healthcare worldwide. If you are seeking a rewarding opportunity within a globally respected organization, we encourage you to submit your application today.Learn more about our EEO & Accommodations request here .