Clinical Research Associate

JR Italy; Treviso; In loco; EUR 35.000 - 60.000; Tempo pieno

Descrizione del lavoro

An established industry player is looking for skilled Clinical Research Associates (CRAs) to support a global study starting in Q1 2025. This role involves ensuring high-quality site monitoring activities, managing compliance, and expanding the clinical network. Ideal candidates will have a CRO background and 1-4 years of experience in clinical research, with a strong understanding of ICH GCP and excellent communication skills. Join a dynamic team dedicated to delivering quality projects in a fast-paced environment, where your contributions will directly impact the success of clinical trials.

Competenze

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

Mansioni

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

Conoscenze

Site Monitoring

ICH GCP Knowledge

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 Support Q1 2025

CliniRx has several CRA positions available to support a global study starting in Q1 2025. We are expanding rapidly and offer multiple permanent opportunities to join our team on a global scale. Ideal candidates will have a CRO background with experience across various 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 needs for emerging biotech and pharmaceutical companies, particularly 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 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 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 for 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 will be critical for the successful delivery of our projects and overall organizational success.

Key Success Factors

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