Clinical Research Associate based in Germany

Fortrea; Deutschland; Remote; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

A leading company in clinical research is seeking a Clinical Research Associate (CRA) to oversee clinical trial sites across various therapeutic areas. This role involves managing compliance and data integrity while collaborating with diverse teams. With opportunities for professional development and a flexible work model, this position is ideal for detail-oriented candidates committed to advancing patient outcomes.

Leistungen

Flexible work model

Competitive benefits

Commitment to employee well-being

Qualifikationen

• Solid understanding of ICH-GCP guidelines and local regulatory requirements.
• Proficient in using clinical systems and tools; able to work independently.

Aufgaben

• Manage clinical trial sites in alignment with SOPs, ICH-GCP, and sponsor requirements.
• Conduct all phases of site monitoring visits ensuring subject safety and data integrity.
• Collaborate with cross-functional teams to align site performance with study timelines.

Kenntnisse

Attention to detail

Clinical trial processes

Monitoring procedures

Ausbildung

University or college degree in life sciences, nursing, pharmacy, or a related allied health profession

Tools

Clinical systems

Jobbeschreibung

Be the connection between science and solutions. In this CRA position, you’ll 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 Fortrea’s 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.

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