Clinical Research Associate

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

Descrizione del lavoro

An established industry player is seeking skilled Clinical Research Associates (CRAs) to support a global study in Q1 2025. This role offers permanent opportunities within a rapidly expanding contract research organization. Candidates will play a crucial role in ensuring high-quality site monitoring activities, adhering to strict timelines, and maintaining compliance with regulations. The ideal candidate will possess a strong background in clinical research, excellent communication skills, and a commitment to quality. Join a dynamic team that values your contributions and offers the chance to grow in a supportive environment.

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 and regulations.
• Assist in identifying new potential sites across various therapeutic areas.

Conoscenze

Site Monitoring

Communication Skills

Multitasking

Knowledge of ICH GCP

Clinical Trial Regulations

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 multiple CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer 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 provide a diverse range of clinical development and resource solutions, including 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 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 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 quality and adherence to timelines.
2. Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize 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 improve technical and soft skills to enhance 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 timeliness in monitoring activities is vital for the successful delivery of our projects.

Key Success Factors

• Timely and 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 clinical trial regulations; excellent communication skills; ability to multitask under tight deadlines.