Clinical Research Associate

JR Italy; Torino; In loco; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

An established industry player in clinical research is seeking skilled Clinical Research Associates (CRAs) to ensure high-quality site monitoring for global studies. This role offers the opportunity to work on diverse clinical development projects, supporting biotech and pharmaceutical companies. As a CRA, you'll play a critical role in managing site compliance and enhancing project outcomes through your expertise in ICH GCP regulations and strong communication skills. Join a dynamic team and contribute to impactful clinical trials that shape the future of healthcare.

Competenze

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

Mansioni

• Ensure adherence to the Site Monitoring Plan and quality standards.
• Manage site compliance and minimize QA audit observations.
• Identify new potential sites to expand the clinical network.

Conoscenze

Site Monitoring

ICH GCP Regulations

Communication Skills

Multitasking

Formazione

Bachelor’s Degree in Scientific Discipline

Master’s Degree in Scientific Discipline

Descrizione del lavoro

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CliniRx has a number of CRA positions available to support a global study in Q1 2025.

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 diverse 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. Our presence includes 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 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 is crucial for the successful delivery of our projects.

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 in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and applicable regulations; excellent communication skills; ability to multitask and work under demanding timelines.