Junior Clinical Research Associate — Site Monitoring & Trials

IQVIA; Paris; Sur place; EUR 52 000 - 75 000; Plein temps

Résumé du poste

IQVIA, a leading global provider of clinical research services, seeks a CRA to monitor and manage study sites, ensure protocol adherence, and maintain regulatory compliance across trials. You will coordinate with sites, manage recruitment plans, and document findings throughout the TMF/ISF lifecycle.

The role emphasizes strong communication, organization, and time management skills, with opportunities to contribute to start-up activities and financial oversight as needed.

Qualifications

• Bachelor's degree in a scientific discipline or healthcare.
• Equivalent combination of education, training and experience may be accepted.
• Some organizations require CRA training or prior monitoring experience.
• Basic knowledge of GCP/ICH regulatory requirements.
• Good written and verbal English communication.

Responsabilités

• Conduct site monitoring visits per contracted scope and regulatory requirements.
• Support subject recruitment plans to meet project needs.
• Administer protocol training to assigned sites and maintain regular communication.
• Evaluate site practices for quality and protocol adherence; escalate issues.
• Track regulatory submissions, approvals, recruitment, data queries and resolution.
• Ensure TMF/ISF documents are maintained and filed in compliance.
• Create visit reports and follow-up letters; maintain study documentation.
• Collaborate with study team for project execution support.
• Support start-up activities and site financial management where applicable.

Connaissances

Communication skills

Organizational skills

Time management

Formation

Bachelor's degree in scientific discipline or healthcare

Outils

MS Word

MS Excel

PowerPoint

Laptop

iPhone/iPad

Description du poste

IQVIA, a leading global provider of clinical research services, seeks a CRA to monitor and manage study sites, ensure protocol adherence, and maintain regulatory compliance across trials. You will coordinate with sites, manage recruitment plans, and document findings throughout the TMF/ISF lifecycle.

The role emphasizes strong communication, organization, and time management skills, with opportunities to contribute to start-up activities and financial oversight as needed.