Lead CRA: Clinical Monitoring & Site Management

Fortrea; Paris; Hybride; EUR 45 000 - 65 000; Plein temps

Résumé du poste

A global healthcare organization is seeking a Clinical Monitor to oversee site management for clinical trials. The candidate will ensure compliance with ICH GCP guidelines, conduct site monitoring, and manage project plans. Ideal candidates have a degree in a health-related field and at least 2 years of clinical monitoring experience. This role is full-time and requires travel up to 60% of the time.

Qualifications

• 2+ years of Clinical Monitoring experience.
• Thorough knowledge of monitoring procedures.
• Good analytical and negotiation skills.

Responsabilités

• Conduct site monitoring responsibilities for clinical trials.
• Ensure adherence to regulatory requirements.
• Prepare and implement project plans related to Clinical Monitoring.

Connaissances

Thorough understanding of ICH GCP Guidelines

Fluent in English

Good understanding of medical and clinical research terminology

Formation

University or college degree or certification in a related allied health profession

Outils

e-clinical systems

Description du poste

A global healthcare organization is seeking a Clinical Monitor to oversee site management for clinical trials. The candidate will ensure compliance with ICH GCP guidelines, conduct site monitoring, and manage project plans. Ideal candidates have a degree in a health-related field and at least 2 years of clinical monitoring experience. This role is full-time and requires travel up to 60% of the time.