Unblinded CRA based in Germany (Ruhrgebiet)
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 9h 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 30d ago
The date the source published, not the day we noticed it (2026-09-02). Last seen at its source just now.
We have tracked this listing since 22 Sep 2026 (9 days). The employer's board dropped it once and re-listed it; it was last seen there 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.
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 9d ago · last seen just now
- location not stated
The listing
Key Responsibilities
- You will perform unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product oversight
- You will ensure protocol compliance, data integrity, and patient safety at assigned sites
- You will maintain accurate and complete study documentation, including eTMF and regulatory files
- You will build strong relationships with site staff, acting as the primary point of contact for site management (pharmacy only)
- You could contribute to audit readiness and ensure inspection preparedness at site level
Required Qualifications
- Bachelor’s degree in Life Sciences or related field (or equivalent experience)
- Initial experience in clinical research as a CRA with at least 1 year of monitoring experience
- Understanding of ICH-GCP guidelines and clinical trial processes
- Strong interest and knowledge in unblinded study conduct and Investigational Product management
- Fluency in German and English (written and spoken)
- Willingness to travel within Germany and Austria as required
- Strong organizational skills with attention to detail
What We Offer
- Opportunity to work in a sponsor-dedicated environment on innovative studies
- Structured onboarding and continuous development programs
- Flexible working model supporting work-life balance
- Access to global career growth opportunities within clinical operations
- Inclusive and collaborative culture with employee resource groups and wellbeing initiatives
#LI-GQ1 #LI-Remote
Learn more about our EEO & Accommodations request here.