Clinical Research Associate I/II (CRA)

1w1 week ago

Fortrea

Munich, DE · Full-time · €45,000 – €65,000

About this role

Be the connection between science and solutions as a Clinical Research Associate I or II. Take your first or next step into clinical research, supporting successful delivery of clinical trials under guidance of experienced colleagues. This role suits early-career professionals with up to 1 year of onsite monitoring experience in a structured environment.

Contribute to execution of clinical studies across Oncology, Dermatology, Respiratory, Cardiology, and Diabetes. Gain broad exposure and hands-on experience developing monitoring skills. This is for upcoming future opportunities at Fortrea.

Support management of clinical trial sites in compliance with Fortrea SOPs, ICH-GCP, study protocols, and sponsor requirements. Assist in site initiation, routine monitoring, and close-out visits ensuring patient safety and protocol adherence. Collaborate with cross-functional teams and escalate issues to contribute to site performance and timelines.

Grow your career in a structured and supportive environment with clear development pathways and mentoring. Benefit from formal training programs, modern clinical systems, and continuous learning. Enjoy a flexible work model, competitive benefits, and a culture valuing collaboration, quality, and well-being.

Requirements

University or college degree in life sciences, nursing, pharmacy, or a related field; relevant internships or equivalent experience considered
Entry-level to 1 year of experience in clinical research, including internships, trainee roles, or up to 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

Responsibilities

Support management of clinical trial sites in compliance with Fortrea SOPs, ICH-GCP, study protocols, and sponsor requirements, with appropriate supervision
Assist in 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 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

Benefits

Grow 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 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