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 execution
What 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 skills
Location: 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.