Clinical Research Associate Freelance - Remote

Buscojobs; Friuli-Venezia Giulia; Remoto; EUR 30.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading clinical research organization is seeking a Clinical Research Associate (CRA) to ensure high-quality monitoring of clinical trials. You will drive site monitoring plans, conduct visits, and ensure compliance with regulatory standards. The ideal candidate has a degree in Life Sciences and 1–4 years of experience in site monitoring. This role is 100% remote and offers opportunities for professional growth.

Competenze

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

Mansioni

• Drive the site monitoring plan and ensure high-quality delivery.
• Conduct site initiation, monitoring, and closeout visits.
• Perform Source Document Verification and ensure regulatory compliance.
• Collaborate with investigators to ensure protocol adherence.
• Support sites with training and audit readiness.
• Identify and engage potential new sites.

Conoscenze

Site monitoring

Compliance

Communication

Multitasking

Problem-solving

Formazione

Graduate/Postgraduate in Life Sciences

Descrizione del lavoro

Overview

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.