At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for aClinical Research Associate (CRA)who shares our passion for excellence and is ready to make a real impact in advancing clinical research. What You’ll Do:Drive thesite monitoring planby ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans. Conductsite initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements. PerformSource Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy. Collaborate with investigators to ensure adherence toprotocols, regulatory guidelines, and ICH GCPstandards. Support sites with training, essential document collection, and audit/inspection readiness. Identify and engage potential new sites across therapeutic areas.Who You’ll Work With:You’ll collaborate closely with ourProject Managers, Clinical Operations team, site personnel, and QA teamsto ensure seamless study delivery. What Success Looks Like:High-quality and timely site monitoring Accurate and compliant documentation Strong site engagement and smooth study executionWhat We’re Looking ForGraduate/Postgraduate inLife Sciences 1–4 yearsof experience in site monitoring Strong knowledge ofICH GCP and clinical trial regulations Excellent communication, multitasking, and problem-solving skillsLocation:100% Remote (Home-Based)At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.