PAt CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a bClinical Research Associate (CRA) /b who shares our passion for excellence and is ready to make a real impact in advancing clinical research. /ppbr/ppbWhat You’ll Do: /b /ppbr/pulliDrive the bsite monitoring plan /b by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans. /liliConduct bsite initiation, monitoring, and closeout visits /b, ensuring all activities comply with SOPs and regulatory requirements. /liliPerform bSource Document Verification (SDV) /b, review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy. /liliCollaborate with investigators to ensure adherence to bprotocols, regulatory guidelines, and ICH GCP /b standards. /liliSupport sites with training, essential document collection, and audit/inspection readiness. /liliIdentify and engage potential new sites across therapeutic areas. /li /ulpbr/ppbWho You’ll Work With: /b /ppbr/ppYou’ll collaborate closely with our bProject Managers, Clinical Operations team, site personnel, and QA teams /b to ensure seamless study delivery. /ppbWhat Success Looks Like: /b /ppbr/pulliHigh-quality and timely site monitoring /liliAccurate and compliant documentation /liliStrong site engagement and smooth study execution /li /ul pbWhat We’re Looking For /b /ppbr/pulliGraduate/Postgraduate in bLife Sciences /b /lilib1–4 years /b of experience in site monitoring /liliStrong knowledge of bICH GCP and clinical trial regulations /b /liliExcellent communication, multitasking, and problem-solving skills /li /ulpbr/ppb Location: /b 100% Remote (Home-Based) /ppbr/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