Clinical Research Associate

JR Italy; Chieti; In loco; EUR 30.000 - 60.000; Tempo pieno

Descrizione del lavoro

An innovative global contract research organization is seeking skilled Clinical Research Associates (CRAs) to join their expanding team for a global study in 2025. This role involves ensuring the timely and high-quality delivery of site monitoring activities, adhering to strict protocols and regulations. The ideal candidate will have a strong background in clinical research, excellent communication skills, and the ability to multitask effectively. Join a dynamic team committed to supporting biotech and pharmaceutical companies in overcoming unique challenges in clinical development.

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 the Site Monitoring Plan and project timelines.
• Manage sites to minimize Quality Assurance audit observations.
• Identify new potential sites to expand the clinical network.

Conoscenze

Site Monitoring

Clinical Research

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 - Global Study 2025

CliniRx has several CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer multiple permanent opportunities to join our team on a global study. Candidates with a CRO background and experience across multiple therapeutic areas are preferred.

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 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 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 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 regarding project, functional, and administrative matters.
• Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.

Value Added

Your commitment to quality and adherence to timelines is vital for the successful delivery of our projects.

Key Success Factors

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