Clinical Research Associate based in Germany or in Austria

CHEManager International; München; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A global clinical research organization in Bavaria is seeking a Clinical Research Associate (CRA) to manage clinical trial sites in compliance with regulatory standards. You'll influence the success of global trials and work on various indications like oncology and cardiology. The ideal candidate has a degree in life sciences and fluency in German and English. This role offers a flexible work model and focuses on improving patient outcomes through innovative therapies.

Leistungen

Flexible work model

Competitive benefits

Professional development opportunities

Qualifikationen

• University or college degree in life sciences or related fields.
• Solid understanding of ICH‑GCP guidelines.
• Working knowledge of clinical trial processes.
• Strong attention to detail and ability to follow protocols.
• Fluent in German and English, both written and verbal.
• Proficient in using clinical systems and able to travel.

Aufgaben

• Manage clinical trial sites in compliance with SOPs and regulations.
• Conduct all phases of site monitoring visits.
• Perform source data verification and query resolution.
• Maintain and update essential documents.
• Monitor investigational product accountability.
• Collaborate with cross-functional teams.

Kenntnisse

Attention to detail

Fluent in German

Fluent in English

Strong protocol adherence

Ausbildung

University or college degree in life sciences, nursing, pharmacy

Tools

Clinical systems and tools

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.

This role is for upcoming future opportunities that may arise at Fortrea.

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.

Learn more about our EEO & Accommodations request here.