PAt 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. /ppWhat You’ll Do: /pulliDrive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans. /liliConduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements. /liliPerform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy. /liliCollaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards. /liliSupport sites with training, essential document collection, and audit/inspection readiness. /liliIdentify and engage potential new sites across therapeutic areas. /li /ulpWho You’ll Work With: /ppYou’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery. /ppWhat Success Looks Like: /pulliHigh-quality and timely site monitoring /liliAccurate and compliant documentation /liliStrong site engagement and smooth study execution /li /ulpWhat We’re Looking For /pulliGraduate/Postgraduate in Life Sciences /lili1–4 years of experience in site monitoring /liliStrong knowledge of ICH GCP and clinical trial regulations /liliExcellent communication, multitasking, and problem-solving skills /li /ulp Location: 100% Remote (Home-Based) /ppAt 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. /p