Clinical Research Associate

JR Italy; Ascoli Piceno; In loco; EUR 30.000 - 60.000; Tempo pieno

Descrizione del lavoro

An established industry player is looking for skilled Clinical Research Associates to join their expanding team. This role involves ensuring timely and quality delivery of site monitoring activities, managing compliance, and identifying new clinical sites. With a focus on quality standards and collaboration with various teams, this position offers a unique opportunity to contribute to impactful clinical research projects. If you have a background in CRO and are passionate about advancing healthcare, 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 clinical trial regulations.

Mansioni

• Deliver on the Site Monitoring Plan to ensure quality standards.
• Assist in identifying new potential sites for clinical trials.

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

Job Description

CliniRx has multiple Clinical Research Associate (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. Candidates with a CRO background and experience across multiple therapeutic areas are preferred.

As a global contract research organization (CRO), we provide diverse 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, with a presence in 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 quality delivery of site monitoring activities in line 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 improve technical and soft skills to enhance performance and project outcomes.

Work Relations

• Report to the Manager of Clinical Operations on 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 standards and timelines is crucial 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 in site monitoring within clinical research.
• Skills: Strong understanding of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask under demanding timelines.