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 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.
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