Clinical Research Associate

CliniRx; Rimini; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading global contract research organization is seeking Clinical Research Associates to support a global study starting in Q1 2025. The role involves ensuring high-quality site monitoring, compliance with regulations, and collaboration with various teams. Candidates should have a degree in a scientific discipline and experience in clinical research.

Competenze

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

Mansioni

• Deliver on the Site Monitoring Plan and ensure adherence to quality and timelines.
• Manage sites according to the SMMP and relevant regulations.
• Assist in identifying new potential sites across various therapeutic areas.

Conoscenze

Communication

Multitasking

Understanding of ICH GCP

Formazione

Bachelor’s or Master’s degree in a scientific discipline

Descrizione del lavoro

CliniRx - Clinical Research Associate Positions

CliniRx has multiple CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer several 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 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 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 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 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.
5. Work Relations: Report to the Manager of Clinical Operations and collaborate with site monitoring teams, site personnel, HR, and administrative staff.

Value Added

Your commitment to quality and adherence to timelines will be crucial for the efficient delivery of our projects and overall success.

Key Success Factors

• Timely and high-quality execution of site monitoring activities.
• Prompt report generation and submission to stakeholders.

Essential Skills and Experience

• 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 applicable clinical trial regulations; excellent communication skills; ability to multitask and work under demanding timelines.

Location: Rimini, Italia