Research Associate

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

Résumé du poste

A leading global contract research organization is seeking Clinical Research Associates (CRAs) to join their expanding team. The role involves ensuring high-quality site monitoring activities and compliance with regulations. Ideal candidates will have a scientific background and experience in clinical research. This position offers a chance to contribute to global studies and enhance your skills in a dynamic environment.

Qualifications

• 1-4 years of experience in site monitoring within clinical research.

Responsabilités

• Ensure adherence to the Site Monitoring Plan and project timelines.
• Manage sites according to regulations to minimize QA audit observations.
• Assist in identifying new potential sites.

Connaissances

Communication

Multitasking

Formation

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

Description du poste

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Job Description:

CliniRx has a number of CRA positions available. We are expanding rapidly 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 areas.

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. We support clinical outsourcing needs for emerging biotech and pharmaceutical companies—most notably small to mid-size enterprises facing unique challenges. 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 high-quality delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP).

Key Responsibilities:

1. 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.
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 both technical and soft skills, applying them to elevate performance and project outcomes.
5. 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.

Essential Skills & Experience:

• 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.

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