Clinical Research Associate based in Germany or in Austria
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 4h 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 16h ago
The date the source published, not the day we noticed it (2026-10-02). Last seen at its source just now.
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, Vienna
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.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
workday employer's own board first seen 4h ago · last seen just now
- location not stated
The listing
Be the connection between science and solutions. As a Clinical Research Associate, you will take the next step in your clinical research career, supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with at least one year of onsite monitoring experience who are eager to further develop their skills in a structured and supportive environment.
You will contribute to the execution of clinical studies across a variety of therapeutic areas, including Oncology, Dermatology, Respiratory, Cardiology, and Diabetes, gaining broad exposure and hands‑on experience while developing your monitoring skills.
Key Responsibilities:
Support the management of clinical trial sites in compliance with Fortrea SOPs, ICH‑GCP, study protocols, and sponsor requirements, with appropriate supervision.
Assist in the preparation and conduct of site monitoring activities, including site initiation, routine monitoring, and close‑out visits, ensuring patient safety and protocol adherence.
Perform source data verification (SDV), support query resolution, and review eCRFs to help ensure data quality and completeness.
Maintain and update essential trial documentation in eTMF and sponsor systems to support inspection readiness.
Support investigational product (IP) tracking and accountability checks in collaboration with the study team.
Collaborate with cross‑functional teams and escalate issues appropriately, contributing to site performance, quality, and timelines.
Required Qualifications :
University or college degree in life sciences, nursing, pharmacy, or a related field; relevant internships or equivalent experience will be considered.
Minimum of 12 months of onsite monitoring experience
Basic understanding of ICH‑GCP guidelines and clinical trial processes.
Strong attention to detail, willingness to learn, and ability to follow established procedures and documentation standards.
Fluency in German and English, both written and spoken.
Comfortable using clinical systems and tools, with openness to travel as required for site visits.
Why Join Us?
Grow your clinical research career in a structured and supportive environment with clear development pathways and mentoring.
Gain hands‑on exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills.
Benefit from formal training programs, modern clinical systems, and continuous learning opportunities.
Enjoy a flexible work model, competitive benefits, and a culture that values collaboration, quality, and well‑being.
We welcome applications from early‑career candidates who are motivated to build a career in clinical research and grow with Fortrea. If you are curious, detail‑oriented, and eager to make an impact on patients’ lives, we encourage you to apply.
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