Junior Clinical Research Associate - Site Monitoring

IQVIA; Paris; On-site; EUR 42,000 - 65,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to monitor clinical sites, ensure protocol compliance, and support data integrity for studies. You will perform site visits, manage communications with investigators, and track progress across regulatory submissions and patient recruitment.

The role requires knowledge of GCP/ICH guidelines, strong organizational skills, and ability to work with cross-functional teams. Based in Paris, on-site engagement is expected.

Qualifications

• Bachelor's degree or equivalent in science/health care; CRA training preferred.

Responsibilities

• Perform site monitoring visits (initiation, monitoring, close-out) per scope of work and GCP/ICH guidelines.
• Collaborate with sites to drive and track recruitment plans to meet project needs.
• Administer protocol and study training to sites; maintain regular communication.
• Assess site practices for protocol compliance and regulatory adherence; escalate issues.
• Track regulatory submissions, approvals, recruitment, CRF completion, data queries; support start-up if needed.
• Ensure TMF/ISF documents are filed per GCP/ICH and local requirements.
• Document site management findings and action plans; submit visit reports and follow-up letters.
• Collaborate with study team for project execution support; assist in recruitment planning and site budgeting as applicable.

Skills

Communication

Organizational skills

Problem solving

Time management

Relationship building

Education

Bachelor's degree in scientific discipline or health care

Equivalent combination of education, training and experience

CRA training considered a plus

Tools

MS Word

MS Excel

PowerPoint

iPhone/iPad use (where applicable)

Job description

IQVIA is seeking a Clinical Research Associate to monitor clinical sites, ensure protocol compliance, and support data integrity for studies. You will perform site visits, manage communications with investigators, and track progress across regulatory submissions and patient recruitment.

The role requires knowledge of GCP/ICH guidelines, strong organizational skills, and ability to work with cross-functional teams. Based in Paris, on-site engagement is expected.