Clinical Research Associate

JR France; Colmar; 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. Ideal candidates will have a scientific background and experience in clinical research. Join a dynamic team focused on delivering efficient clinical development solutions.

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 high-quality delivery of site monitoring activities.
• Manage sites according to the Site Monitoring Master Plan 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 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—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 CRAs to ensure the timely and high-quality delivery of site monitoring activities in accordance with our Site Monitoring Plan (SMP).

Key Responsibilities:

• 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.
• 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 across various therapeutic areas to expand our clinical network.
• 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: Adherence to quality and timelines in monitoring activities 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 of experience in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication skills; ability to multitask and work under demanding timelines.