Clinical Research Associate

JR Italy; Parma; In loco; EUR 35.000 - 65.000; Tempo pieno

Descrizione del lavoro

An established industry player in clinical research is seeking skilled Clinical Research Associates (CRAs) to join their expanding team. This role focuses on ensuring the timely and high-quality delivery of site monitoring activities for a global study. Candidates should have a strong background in clinical research, particularly in site monitoring, and be adept at managing multiple tasks under tight deadlines. You will collaborate with various teams to enhance project outcomes while adhering to regulatory standards. If you are passionate about improving clinical trials and thrive in a dynamic environment, this opportunity is perfect for you.

Competenze

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

Mansioni

• Ensure adherence to the Site Monitoring Plan and project timelines.
• Manage sites to minimize Quality Assurance audit observations.
• Identify new potential sites to expand the clinical network.

Conoscenze

Site Monitoring

Clinical Research

ICH GCP

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

We are expanding rapidly and offer 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 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, especially small to mid-size enterprises facing unique challenges, with a presence in key markets including 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 alignment 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 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 within 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 adherence to quality and timelines in monitoring activities will be 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 of site monitoring experience in clinical research.
• Skills: Strong understanding of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask and work under demanding timelines.