Clinical Research Associate

JR Italy; Rovigo; In loco; EUR 40.000 - 70.000; Tempo pieno

Descrizione del lavoro

An established industry player in clinical research is seeking skilled Clinical Research Associates (CRAs) to join their dynamic team for a global study starting in Q1 2025. This role offers permanent opportunities within a rapidly expanding organization, where your expertise in site monitoring will be crucial to the success of clinical trials. Collaborate with a dedicated team, enhance your skills, and contribute to impactful projects that support biotech and pharmaceutical companies worldwide. If you have a background in clinical research and a passion for quality, this is the perfect opportunity for you.

Competenze

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

Mansioni

• Ensure adherence to quality standards and timelines in site monitoring.
• Manage sites according to the Site Monitoring Master Plan.

Conoscenze

Site Monitoring

ICH GCP

Communication Skills

Multitasking

Formazione

Bachelor's degree in a scientific discipline

Master's degree in a scientific discipline

Descrizione del lavoro

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CliniRx CRA Positions for Global Study in Q1 2025

CliniRx has multiple CRA positions available to support a global study starting in Q1 2025.

We are expanding rapidly and offer permanent opportunities to join us on this global study. Ideally, candidates will come from a CRO background with experience across multiple therapeutic areas.

As a global contract research organization (CRO), we provide a diverse range of clinical development and resource solutions, including full-service CRO and functional service provider (FSP) models. We support clinical outsourcing for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises, with a presence in 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 high-quality delivery of site monitoring activities in accordance with our Site Monitoring Plan (SMP).

Key Responsibilities

1. 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.
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 across various therapeutic areas to expand our clinical network.
4. 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

Your adherence to quality standards and timelines 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 communication skills; ability to multitask and work under demanding timelines.