Clinical Research Associate

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

Descrizione del lavoro

An established industry player is expanding rapidly and seeks skilled Clinical Research Associates (CRAs) to join their dynamic team. In this role, you will ensure the timely and high-quality delivery of site monitoring activities, adhering to the Site Monitoring Plan. This position offers a unique opportunity to contribute to global studies and collaborate with various stakeholders in the clinical research field. If you have a CRO background and are passionate about making a difference in clinical development, this is the perfect opportunity for you!

Competenze

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

Mansioni

• Deliver on the Site Monitoring Plan to ensure adherence to quality standards.
• Manage sites according to the SMMP and relevant regulations.

Conoscenze

Site Monitoring

ICH GCP

Verbal Communication

Written Communication

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 have 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 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.

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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 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 efficient delivery and success 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 of experience in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask and perform under demanding timelines.