Clinical Research Associate

JR France; Villeurbanne; Sur place; EUR 40 000 - 55 000; Plein temps

Résumé du poste

A leading global contract research organization is seeking skilled Clinical Research Associates (CRAs) to join their team. The role involves ensuring timely and qualitative delivery of site monitoring activities, managing compliance, and contributing to site identification. Ideal candidates should possess a scientific degree and relevant experience in clinical research.

Qualifications

• 1-4 years in site monitoring within clinical research.
• Strong understanding of ICH GCP and clinical trial regulations.

Responsabilités

• Deliver on the Site Monitoring Plan and ensure adherence to quality.
• Manage sites according to the SMMP and relevant regulations.
• Assist in identifying new potential sites across various therapeutic areas.

Connaissances

Communication

Multitasking

Formation

Bachelor’s or Master’s degree in a scientific discipline

Description du poste

Job Description:

CliniRx has multiple CRA positions available. We are expanding rapidly and offer permanent opportunities to join us on a global study.

Ideally, candidates will have a CRO background with experience across multiple therapeutic areas.

As a global contract research organization (CRO), we provide a diverse range of clinical development and resource solutions, supporting clinical outsourcing for emerging biotech and pharmaceutical companies. We have a presence in key markets including the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

Primary Purpose:

We are seeking skilled CRAs to ensure the timely and qualitative delivery of site monitoring activities in line with our Site Monitoring Plan (SMP).

Key Responsibilities:

• Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines.
• Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize QA audit observations.
• Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.
• Continuous Skill Development: Regularly improve technical and soft skills to enhance performance and project outcomes.

Work Relations:

• Report to the Manager of Clinical Operations for project, functional, and administrative matters.
• Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.

Value Added:

Your adherence to quality and timelines is crucial for the efficient delivery of our projects and overall success.

Key Success Factors:

• Timely and high-quality site monitoring activities.
• Prompt report generation and submission to stakeholders.
• Education: Bachelor’s or Master’s degree in a scientific discipline.
• Experience: 1-4 years in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask under demanding timelines.