Be the connection between science and solutions. As a Clinical Research Associate II, 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.
This role is for upcoming future opportunities that may arise at 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 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
.