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Senior CRA II Sponsor Dedicated based in Düsseldorf region
Job Location:
Monthly Salary:
Posted:
30 May 2026 (30+ days ago)
Posted:
Application Deadline:
14 October 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Join Fortrea as a Senior Clinical Research Associate II within a sponsor-dedicated model where you will work exclusively with a leading global biopharmaceutical this role you will support the delivery of high-quality clinical trials across innovative therapies building strong site relationships and ensuring excellence in study execution.
Working in this model offers close collaboration with the sponsors teams strong study ownership and the opportunity to contribute directly to advancing cutting-edge treatments for patients worldwide.
Core responsibilities:
- Act as primary contact for assigned clinical trial sites building strong collaborative relationships
- Manage site lifecycle from start-up through monitoring and close-out ensuring delivery to timelines and quality standards
- Conduct on-site and remote monitoring identifying risks and driving timely issue resolution
- Ensure compliance with study protocol ICH-GCP and local regulatory requirements
- Oversee site performance including data quality recruitment training and documentation completeness
- Support study execution (e.g. feasibility site activation investigator meetings audit readiness)
- Collaborate cross-functionally to implement site strategies and ensure successful trial delivery
Required Qualifications:
- Bachelors degree in Life Sciences or equivalent experience
- 5 years experience in clinical research including site monitoring/site management
- Proven experience in Oncology Ophthalmology Gene Therapy or similar therapeutic area
- Strong knowledge of ICH-GCP regulatory requirements and clinical trial processes
- Solid problem-solving and critical thinking skills
- Proficiency in German and in English
- Willingness to travel
Join Fortrea and take ownership of clinical trial sites across innovative therapies playing a critical role in delivering high-quality data and accelerating drug development. This role offers strong autonomy cross-functional collaboration and exposure to cutting-edge clinical research.
If you are passionate about advancing clinical research and want to grow your expertise in a sponsor-dedicated environment we encourage you to apply and join us in making a meaningful impact on patients
#LI-GQ1 #LI-Remote
Learn more about our EEO & Accommodations request here.
Required Experience:
Senior IC
