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.
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, we encourage you to apply.
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Learn more about our EEO & Accommodations request here.
Skills Required
- University or college degree in life sciences, nursing, pharmacy, or related field
- Entry-level to 1 year of experience in clinical research including internships or onsite monitoring
- Basic understanding of ICH-GCP guidelines and clinical trial processes
- Fluency in German and English, both written and spoken
- Strong attention to detail and willingness to learn
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
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