Clinical Research Associate (CRA)

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 organisational 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,minimising travel while maximising your impact. Collaborate with passionate professionals in a supportive environment. Contribute to meaningful research that improves lives. Job Data by YubHub .