Clinical Research Associate based in Germany

FTGER Fortrea Germany GmbH; München; On-site; EUR 54,000 - 70,000; Full time

Job summary

Fortrea Germany GmbH in Munich seeks a Clinical Research Associate to support successful clinical trial delivery under experienced guidance. The role targets professionals with at least one year of onsite monitoring experience who want to advance their skills in a structured, supportive setting.

You'll contribute across therapeutic areas (Oncology, Dermatology, Respiratory, Cardiology, Diabetes) and gain broad hands‑on exposure while developing monitoring capabilities.

Qualifications

• University/college degree in life sciences, nursing, pharmacy, or related field.
• Minimum 12 months of onsite monitoring experience.
• Basic understanding of ICH-GCP guidelines and trial processes.
• Fluent in German and English, written and spoken.

Responsibilities

• Support site management and monitoring in line with SOPs, ICH-GCP, study protocols and sponsor requirements.
• Assist in site initiation, routine monitoring, and close‑out visits with supervision.
• Perform SDV, support query resolution, and review eCRFs for data quality.
• Maintain trial documentation in eTMF and sponsor systems for inspection readiness.
• Support IP tracking and accountability checks with the study team.
• Collaborate cross‑functionally to elevate issues and support timelines.

Skills

Attention to detail

Willingness to learn

Ability to follow procedures

Fluency in German and English

Travel readiness

Comfort with clinical systems/tools

Education

Life sciences/related degree

Tools

eTMF (trial documentation system)

Job description

Be the connection between science and solutions. As a Clinical Research Associate, you will take the next step in your clinical research career, supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is suited for professionals with at least one year of onsite monitoring experience who are eager to further develop their skills in a structured and supportive environment. 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 Fortrea SOPs, ICH‑GCP, study protocols, and sponsor requirements, with appropriate supervision.
• Assist in the preparation and conduct of site monitoring activities, including site initiation, routine monitoring, and close‑out visits, ensuring patient safety and protocol adherence.
• Perform source data verification (SDV), support query resolution, and review eCRFs to help ensure data quality and completeness.
• Maintain and update essential trial documentation in eTMF and sponsor systems to support inspection readiness.
• Support investigational product (IP) tracking and accountability checks in collaboration with the study team.
• Collaborate with cross‑functional teams and elevate issues appropriately, contributing to site performance, quality, and timelines.

Required Qualifications

• University or college degree in life sciences, nursing, pharmacy, or a related field; relevant internships or equivalent experience will be considered.
• Minimum of 12 months of onsite monitoring experience
• Basic understanding of ICH‑GCP guidelines and clinical trial processes.
• Strong attention to detail, willingness to learn, and ability to follow established procedures and documentation standards.
• Fluency in German and English, both written and spoken.
• Comfortable using clinical systems and tools, with openness to travel as required for site visits.

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. We welcome applications from early‑career candidates who are motivated to build a career in clinical research and grow with Fortrea. If you are curious, detail‑oriented, and eager to make an impact on patients’ lives.

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.