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Why this grade This listing scored 54/100, which is a D. It lost the most ground on pay transparency. See the breakdown
- Description depth 20 / 20 How much the posting actually says about the work, measured in characters of real text.
- Freshness 15 / 15 How recently it was posted. Older postings are likelier to be filled or abandoned.
- Remote clarity 8 / 15 Whether "remote" means anywhere, or is quietly restricted to one country.
- Role specificity 6 / 10 Whether the listing is tagged well enough to tell what the role actually is.
- Corroboration 5 / 10 Whether more than one source carries this listing.
- Pay transparency 0 / 25 A published salary range, worth more than any other single factor because it is what a candidate cannot find out without applying.
Every figure above is arithmetic over the posting itself — its salary field, its text, its age, its tags and how many sources carry it. How the grades work →
Research & Development Mid level Full Time
Join a sponsor-dedicated model supporting cutting-edge clinical trials in DACH. As an unblinded Clinical Research Associate (CRA I or CRA II level) , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment.
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 Austria or Germany 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
If you are looking to build your clinical monitoring career within a high-impact and supportive environment, we encourage you to apply and grow with us.
Learn more about our EEO & Accommodations request here.
Originally posted on Himalayas
Apply for this role Opens himalayas.app — the link as listed; we have not yet verified it is the employer's own page
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Where this listing came from
- 14 Oct 2026 Himalayas first sighting
Seen on 1 board over 0 days.