Sponsor Dedicated DACH Clinical Research Associate based in Germany
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 10h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 1d ago
The date the source published, not the day we noticed it (2026-10-01). Last seen at its source 3h ago.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
Germany
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay $109.4k–135k/yr
Middle 50% of 20 listings that do state pay — Healthcare · all levels · EMEA · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Carried by 1 source
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workday employer's own board first seen 10h ago · last seen 3h ago
- location not stated
The listing
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 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.
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.
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