Job Opportunities API

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. 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   2 years 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   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. If you are curious, detail‑oriented, and eager to make an impact on patients’ lives, we encourage you to apply. Learn more about our EEO & Accommodations request here .