Clinical Research Associate

JR France; Nantes; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading global contract research organization is seeking skilled Clinical Research Associates (CRAs) to ensure the timely and high-quality delivery of site monitoring activities. Candidates should have a CRO background and experience in clinical research. This position offers opportunities for growth and development in a dynamic environment.

Qualifications

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

Responsabilités

• Deliver on the Site Monitoring Plan and ensure adherence to quality standards.
• 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

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CliniRx has a number of CRA positions available.

We are expanding rapidly and offer multiple 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, reflecting both full-service CRO and functional service provider (FSP) models. We support clinical outsourcing needs for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises facing unique challenges. Our presence includes key markets such as the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

Primary Purpose

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

Key Responsibilities

1. Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality standards and timelines.
2. Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.
3. Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.
4. Continuous Skill Development: Regularly enhance technical and soft skills to improve 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 standards and timelines is crucial for the efficient delivery of our projects and overall success.

Key Success Factors

• Timely and high-quality execution of 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 applicable clinical trial regulations; excellent verbal and written communication; ability to multitask and work under demanding timelines.