Clinical Research Associate based in Germany
Clinical Research Associate based in Germany
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Be the connection between science and solutions.In this CRA position youll help transform complex clinical protocols into real-world results working alongside a team that values precision integrity and progress. This role will offer you the opportunity to directly influence the success of global clinical trials and the delivery of innovative therapies to patients worldwide. You would be involved in a variety of indications like Oncology Dermatology Respiratory Cardiology Diabetes.
Key Responsibilities:
Manage clinical trial sites in alignment with Fortrea SOPs ICH-GCP project plans and sponsor requirements including oversight of training documentation and regulatory compliance.
Conduct all phases of site monitoring visits (pre-study initiation routine and close-out) ensuring subject safety protocol adherence and data integrity.
Perform source data verification query resolution and eCRF review to ensure high-quality audit-ready clinical data.
Maintain and update essential documents in eTMF and sponsor systems ensuring regulatory and documentation completeness throughout the study lifecycle.
Monitor investigational product (IP) accountability storage and compliance with protocol and regulatory standards.
Collaborate with cross-functional teams to align site performance with study timelines metrics and quality expectations.
Required Qualifications :
University or college degree in life sciences nursing pharmacy or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
Solid understanding of ICH-GCP guidelines and local regulatory requirements governing clinical research.
Working knowledge of clinical trial processes and monitoring procedures.
Strong attention to detail and ability to follow complex protocols and documentation standards.
Fluent in German and in English both written and verbal.
Proficient in using clinical systems and tools; able to work independently and travel as required.
Why Join Us
Contribute to advancing innovative therapies and improving patient outcomes through meaningful clinical research on a global scale.
Thrive in a collaborative environment that values continuous learning mentorship and professional development.
Work with modern clinical technologies and streamlined systems that support efficiency quality and compliance.
Benefit from a flexible work model competitive benefits and a strong commitment to employee well-being.
We invite qualified candidates who are committed to excellence in clinical research to apply and become part of Fortreas mission to advance healthcare worldwide. If you are seeking a rewarding opportunity within a globally respected organization we encourage you to submit your application today.
#LI-GQ1 #LI-Remote
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
Employment Type
Full-Time
