Clinical Research Associate

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

Descrizione del lavoro

An established industry player is seeking skilled Clinical Research Associates (CRAs) to join their rapidly expanding team. This role offers an exciting opportunity to contribute to global studies while ensuring the highest quality in site monitoring activities. You will be part of a dynamic environment, collaborating with various stakeholders to enhance clinical operations. With a commitment to quality and timely execution, you will play a crucial role in delivering successful projects. If you have a background in clinical research and a passion for excellence, this is the perfect opportunity for you.

Competenze

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

Mansioni

• Ensure timely and high-quality delivery of site monitoring activities.
• Manage sites according to the Site Monitoring Master Plan.

Conoscenze

Site Monitoring

Clinical Research

Communication Skills

Regulatory Knowledge (ICH GCP)

Multitasking

Formazione

Bachelor’s Degree in a Scientific Discipline

Master’s Degree in a 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 a diverse range of 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—most notably 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.

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Primary Purpose:

We are seeking skilled CRAs to ensure the timely and high-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 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 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 timely execution of monitoring activities is crucial for the successful delivery of our projects.

Key Success Factors:

• Timely, high-quality 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 knowledge of ICH GCP and applicable clinical trial regulations; excellent communication skills; ability to multitask and perform under tight deadlines.