At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical 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 the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans. - Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements. - Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy. - Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards. - 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 our Project Managers, Clinical Operations team, site personnel, and QA teams to 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 For- Graduate/Postgraduate in Life Sciences - 1–4 years of experience in site monitoring - Strong knowledge of ICH 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.