Clinical Research Associate

JR France; Laval; Sur place; EUR 35 000 - 50 000; Plein temps

Résumé du poste

A leading global contract research organization is seeking skilled Clinical Research Associates (CRAs) to ensure high-quality site monitoring activities. The role involves delivering on the Site Monitoring Plan, managing compliance, and identifying new sites. Ideal candidates will have a scientific degree and 1-4 years of relevant experience, with strong communication and multitasking skills.

Qualifications

• 1-4 years in site monitoring within clinical research.
• Strong understanding of ICH GCP and applicable clinical trial regulations.
• Excellent communication skills; ability to multitask and meet demanding timelines.

Responsabilités

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

Connaissances

Communication

Multitasking

Understanding of ICH GCP

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 have multiple permanent opportunities to join us on a global study.

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

As a global contract research organization (CRO), we offer 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 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 alignment 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 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 within 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 and timelines in monitoring will be 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 communication skills; ability to multitask and meet demanding timelines.