Clinical Research Associate

JR France; Cherbourg-en-Cotentin; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A global contract research organization is seeking Clinical Research Associates in Cherbourg-Octeville. Ideal candidates will have CRO experience and a scientific background. Responsibilities include site monitoring, compliance management, and skill development.

Qualifications

• 1-4 years in clinical site monitoring.
• Knowledge of ICH GCP and clinical trial regulations.

Responsabilités

• Deliver on the Site Monitoring Plan ensuring quality and adherence to timelines.
• Manage sites according to SMMP and regulations.
• Assist in identifying new sites to expand the network.

Connaissances

Communication

Multitasking

Ability to work under pressure

Formation

Bachelor’s or Master’s in a scientific discipline

Description du poste

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Clinical Research Associate, Cherbourg-Octeville

Client:

CliniRx

Location:

Cherbourg-Octeville, France

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

579201409589706752327654

Job Views:

4

Posted:

16.05.2025

Job Description:

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

Ideal candidates will have a CRO background with experience across various therapeutic areas.

As a global contract research organization (CRO), we provide diverse clinical development and resource solutions, supporting biotech and pharmaceutical companies worldwide, with offices in the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

Primary Purpose:

We seek skilled CRAs to ensure timely and quality site monitoring activities in line with our Site Monitoring Plan (SMP).

Key Responsibilities:

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

Work Relations:

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

Value Added:

Your commitment to quality and timelines is essential for project success.

Key Success Factors:

• High-quality, timely site monitoring activities.
• Prompt reporting to stakeholders.
• Education: Bachelor’s or Master’s in a scientific discipline.
• Experience: 1-4 years in clinical site monitoring.
• Skills: Knowledge of ICH GCP, clinical trial regulations, strong communication, multitasking, and ability to work under pressure.