Join a sponsor-dedicated model supporting cutting-edge clinical trials in DACH. As an unblinded Clinical Research Associate , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment.
Key Responsibilities
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You will perform unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product oversight
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You will ensure protocol compliance, data integrity, and patient safety at assigned sites
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You will maintain accurate and complete study documentation, including eTMF and regulatory files
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You will build strong relationships with site staff, acting as the primary point of contact for site management (pharmacy only)
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You could contribute to audit readiness and ensure inspection preparedness at site level
Required Qualifications
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Bachelor’s degree in Life Sciences or related field (or equivalent experience)
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Initial experience in clinical research as a CRA with at least 1 year of monitoring experience
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Understanding of ICH-GCP guidelines and clinical trial processes
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Strong interest and knowledge in unblinded study conduct and Investigational Product management
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Fluency in German and English (written and spoken)
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Willingness to travel within Germany and Austria as required
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Strong organizational skills with attention to detail
What We Offer
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Opportunity to work in a sponsor-dedicated environment on innovative studies
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Structured onboarding and continuous development programs
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Flexible working model supporting work-life balance
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Access to global career growth opportunities within clinical operations
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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.
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