Clinical Research Associate

JR Italy; Varese; 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 join their dynamic team. This role involves ensuring the timely and high-quality delivery of site monitoring activities, adhering to established protocols and regulations. Ideal candidates will have a background in CRO with a solid understanding of ICH GCP and clinical trial regulations. This is a fantastic opportunity to contribute to impactful global studies while enhancing your skills in a supportive environment. Join a forward-thinking organization dedicated to advancing clinical development solutions!

Competenze

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

Mansioni

• Deliver on the Site Monitoring Plan to ensure quality and timeliness.
• Manage sites per regulations to minimize QA audit observations.
• Assist in identifying new potential sites across therapeutic areas.

Conoscenze

Site Monitoring

Clinical Research

ICH GCP Regulations

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 Q1 2025

CliniRx has multiple CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer permanent opportunities to join us on this project. Ideal candidates will have 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 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 quality and timeliness.
2. Site Management Compliance: Manage sites per the SMMP and relevant regulations to minimize 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.
• Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.

Value Added

Your adherence to quality and timelines is crucial for the efficient delivery and success of our projects.

Key Success Factors

• Timely, high-quality site monitoring activities.
• Prompt report generation and submission.
• 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; ability to multitask under demanding timelines.