CRA

CliniRx; Lille; À distance; EUR 20 000 - 40 000; Plein temps

Résumé du poste

A leading clinical research organization is seeking a Site Monitor for a remote position. Responsibilities include driving the site monitoring plan, ensuring compliance with regulations, and supporting sites with training and documentation. The ideal candidate has a degree in Life Sciences and 1–4 years of site monitoring experience, with strong knowledge of ICH GCP regulations. Join a collaborative team to impact global healthcare.

Qualifications

• 1–4 years of experience in site monitoring.
• Strong knowledge of ICH GCP and clinical trial regulations.

Responsabilités

• Drive the site monitoring plan and ensure timely, high-quality delivery.
• Conduct site initiation, monitoring, and closeout visits.
• Perform Source Document Verification and ensure SAE reporting accuracy.

Connaissances

Site monitoring

Communication

Problem-solving

Multitasking

Formation

Graduate / Postgraduate in Life Sciences

Description du poste

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.