Research Associate

JR France; Colmar; Sur place; EUR 40 000 - 55 000; Plein temps

Résumé du poste

A leading global contract research organization is seeking skilled Clinical Research Associates (CRAs) to ensure the timely and qualitative delivery of site monitoring activities. The ideal candidate will have a scientific background and experience in clinical research. This role involves managing site compliance, identifying new sites, and enhancing skills to improve project outcomes.

Qualifications

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

Responsabilités

• Deliver on the Site Monitoring Plan, ensuring 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

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 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. Our presence includes key 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 qualitative 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.