Clinical Research Associate

JR Italy; Pavia; In loco; EUR 40.000 - 80.000; Tempo pieno

Descrizione del lavoro

An established industry player in clinical research is seeking skilled Clinical Research Associates (CRAs) to join their expanding team. This role is crucial for ensuring the timely and quality delivery of site monitoring activities. With opportunities to work on a global study, you will engage in site management, compliance, and continuous skill development. The ideal candidate will have a scientific background and experience in site monitoring, along with a strong understanding of clinical trial regulations. Join this dynamic organization and contribute to impactful projects in the biotech and pharmaceutical sectors.

Competenze

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

Mansioni

• Ensure adherence to the Site Monitoring Plan and quality standards.
• Manage sites to minimize Quality Assurance audit observations.
• Assist in identifying new potential sites across therapeutic areas.

Conoscenze

Site Monitoring

Communication Skills

Multitasking

Knowledge of ICH GCP

Clinical Trial Regulations

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 - Global Study Q1 2025

CliniRx has multiple CRA (Clinical Research Associate) positions available to support a global study starting in Q1 2025. We are expanding rapidly and offer several permanent opportunities to join our team on a global study. Ideally, candidates should 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 needs for emerging biotech and pharmaceutical companies, particularly 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 quality delivery of site monitoring activities in line 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 improve technical and soft skills to enhance 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 in monitoring activities will be vital for the successful delivery of our projects.

Key Success Factors

• Timely and high-quality site monitoring activities.
• Prompt report generation and stakeholder communication.
• Education: Bachelor’s or Master’s degree in a scientific discipline.
• Experience: 1-4 years in site monitoring within clinical research.
• Skills: Strong knowledge of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask and work under demanding timelines.