Clinical Research Associate

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

Résumé du poste

A leading global contract research organization is seeking Clinical Research Associates (CRAs) to join their team. The role involves ensuring the quality and timeliness of site monitoring activities, managing compliance, and identifying new sites. Candidates should have a scientific degree and experience in clinical research, with strong communication skills and an understanding of ICH GCP.

Qualifications

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

Responsabilités

• Ensure timely and qualitative delivery of site monitoring activities.
• 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 have a number of CRA positions available.

We are expanding at a rapid rate and have multiple opportunities on a permanent basis to join us on a global study.

Ideally you will come from a CRO background with experience across multiple therapeutic area's.

As a global contract research organization (CRO), we offer a diverse slate of clinical development and resource solutions reflecting both full-service CRO and functional service provider (FSP) models. In supporting clinical outsourcing needs for emerging biotech and pharmaceutical companies—most notably small to mid-size enterprises facing unique challenges we offer our expertise with a presence in key markets including the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia

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Primary Purpose: We are seeking skilled CRA's to ensure the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP).

Key Responsibilities:

• Deliver on the Site Monitoring Plan: Gain a comprehensive understanding of 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 Quality Assurance (QA) audit observations.
• Site Identification: Assist in identifying new potential sites within various therapeutic areas to expand our clinical network.
• Continuous Skill Development: Regularly enhance both technical and soft skills, applying them to elevate 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 executives.

Value Added:

Your adherence to the quality and timelines of the monitoring plan 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 of experience 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 thrive under demanding timelines.