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Clinical Research Associate I in Germany
Job Location:
Monthly Salary:
Posted:
21 August 2026 (13 days ago)
Posted:
Application Deadline:
18 November 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
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 handson 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 handson 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 wellbeing.
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 wed love to hear from you.
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Learn more about our EEO & Accommodations request here.
Required Experience:
IC
