Clinical Research Associate based in Germany or in Austria

Fortrea; United States; Remote; USD 65,000 - 90,000; Full time

Job summary

Fortrea is seeking a Clinical Research Associate to advance your clinical research career by supporting successful delivery of trials under experienced guidance.

The role suits professionals with at least one year of onsite monitoring experience, eager to grow in a structured, supportive environment with exposure to Oncology, Dermatology, Respiratory, Cardiology, and Diabetes studies.

Qualifications

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

Responsibilities

• Support site management in line with Fortrea 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 essential trial documentation in eTMF and sponsor systems.
• Support IP tracking and accountability checks with the study team.
• Collaborate across teams and escalate issues to protect timelines and quality.

Skills

Onsite monitoring

SDV

ICH-GCP knowledge

Documentation

Site coordination

German language

English language

Education

Life sciences degree

Tools

eTMF familiarity

Clinical systems

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 **escalate** 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.

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