Clinical Research Associate based in Germany

Fortrea; München; Remote; EUR 50.000 - 75.000; Vollzeit

Zusammenfassung

A leading healthcare company is seeking a Clinical Research Associate in Munich to manage trial sites, ensuring compliance with protocols and regulations. You'll contribute to the success of global clinical trials across various indications, including oncology and cardiology. This role offers the chance to work with innovative therapies and contribute to improving patient outcomes globally. Join a collaborative environment where your expertise will enhance clinical research efforts.

Leistungen

Flexible work model

Competitive benefits package

Opportunities for professional development

Supportive collaborative environment

Qualifikationen

• University degree in relevant field or equivalent experience.
• Fluency in German and English, both written and verbal.
• Solid understanding of ICH-GCP guidelines.

Aufgaben

• Manage clinical trial sites and ensure compliance with protocols.
• Conduct site monitoring visits and perform data verification.
• Collaborate with teams to align site performance with study goals.

Kenntnisse

Attention to detail

Protocol adherence

Data integrity

Communication

Ausbildung

Degree in life sciences, nursing, pharmacy, or related field

Tools

Clinical systems and tools

Jobbeschreibung

Clinical Research Associate based in Germany page is loaded

Clinical Research Associate based in Germany

Apply remote type Remote locations Munich Remote Germany time type Full time posted on Posted Today job requisition id 253528

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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At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.