Clinical Research Associate based in Germany

FTGER Fortrea Germany GmbH; München; Vor Ort; EUR 52.000 - 68.000; Vollzeit

Benefits dieser Stelle

Flexible work model

Zusammenfassung

Fortrea Germany GmbH is seeking a Clinical Research Associate to advance the execution of clinical trials across multiple therapeutic areas. The role emphasizes hands‑on monitoring and ensuring patient safety under experienced supervision, with opportunities for growth in a structured environment.

The successful candidate will contribute to SDV, data quality, and trial documentation while collaborating with cross‑functional teams.

Qualifikationen

• University degree in life sciences, nursing, pharmacy or related field.
• Minimum of 12 months of onsite monitoring experience.
• Basic understanding of ICH‑GCP guidelines and clinical trial processes.
• Strong attention to detail and ability to follow procedures.
• Fluency in German and English, both written and spoken.
• Willingness to travel for site visits.

Aufgaben

• Support management of clinical trial sites in compliance with SOPs, ICH‑GCP and study protocols.
• Assist in site monitoring activities including initiation, routine monitoring and close‑out visits.
• Perform source data verification (SDV) and review eCRFs for data quality and completeness.
• Maintain essential trial documentation in eTMF and sponsor systems for inspection readiness.
• Support IP tracking and accountability checks with the study team.
• Collaborate with cross‑functional teams to elevate issues and support timelines.

Kenntnisse

Onsite monitoring experience

Attention to detail

Willingness to learn

German and English fluency

Ausbildung

University or college degree in life sciences, nursing, pharmacy or related field

Tools

eTMF

eCRF

Jobbeschreibung

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.

We welcome applications from early‑career candidates who are motivated to build a career in clinical research and grow with Fortrea.

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.

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.