Clinical Research Associate I in Germany

Fortrea; München; Vor Ort; EUR 48.000 - 70.000; Vollzeit

Zusammenfassung

Fortrea is seeking professionals ready to move into a Clinical Research Associate role in Munich, Germany. You will transition from roles such as Study Nurse or CTA to on‑site monitoring, gaining exposure across oncology, dermatology, and more.

You will support site visits, SDV, and documentation while developing core CRA skills under experienced colleagues. Travel across Germany is part of the role, with formal training and mentoring.

Qualifikationen

• Degree in Life Sciences, Nursing, Pharmacy, or related field.
• Experience in clinical research as Study Nurse, Study Coordinator, CTA, CRA, or similar.
• Fluent in German and English, written and spoken.
• Willingness to travel for onsite monitoring across Germany.

Aufgaben

• Support the management of clinical trial sites in ICH‑GCP compliance.
• Participate in site initiation, routine monitoring, and close‑out visits.
• Conduct SDV and support data review for quality and safety.
• Assist sites with study questions and cross‑functional issue resolution.
• Maintain trial documentation and support eTMF completeness.
• Contribute to site recruitment, quality, and timeline objectives.

Kenntnisse

German language proficiency

English language proficiency

Organizational skills

Willingness to travel

Ausbildung

Degree in Life Sciences, Nursing, Pharmacy, or related scientific discipline

Jobbeschreibung

Are you ready to take the next step in your clinical research career and transition into a Clinical Research Associate role?

We are looking for motivated professionals with experience as a Study Nurse, Study Coordinator, Clinical Trial Assistant (CTA), or In-House CRA who are eager to move into onsite monitoring and build a successful CRA career.

You will contribute to the execution of clinical studies across a variety of therapeutic areas, including Oncology, Dermatology, Respiratory, Cardiology, and Diabetes, gaining broad exposure and hands‑on experience while developing your monitoring skills.

Key Responsibilities

• Support the management of clinical trial sites in compliance with ICH‑GCP, study protocols, sponsor requirements, and Fortrea SOPs.
• Participate in site initiation, routine monitoring, and close‑out visits under the guidance of experienced CRA colleagues.
• Conduct source data verification (SDV) and support data review activities to ensure data quality and patient safety.
• Assist sites with study‑related questions and support issue resolution in collaboration with cross‑functional teams.
• Maintain clinical trial documentation and support eTMF completeness and inspection readiness.
• Contribute to study progress by helping sites meet recruitment, quality, and timeline objectives.

Required Qualifications

• Degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline.
• Experience in clinical research as a Study Nurse, Study Coordinator, CTA, Clinical Trial Associate, In‑House CRA, or similar role.
• Good understanding of clinical trial processes and ICH‑GCP guidelines.
• Strong organizational skills, attention to detail, and a proactive mindset.
• Fluent in German and English, both written and spoken.
• Willingness to travel for onsite monitoring visits across Germany.

Why Join Us?

• Grow your clinical research career in a structured and supportive environment with clear development pathways and mentoring.
• Gain hands‑on exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills.
• Benefit from formal training programs, modern clinical systems, and continuous learning opportunities.
• Enjoy a flexible work model, competitive benefits, and a culture that values collaboration, quality, and well‑being.

At Fortrea, we welcome ambitious clinical research professionals who are ready to make the move into monitoring. If you have experience supporting clinical trials and are looking for your first CRA opportunity, we'd love to hear from you.

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