Clinical Research Associate

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

Descrizione del lavoro

A leading global contract research organization seeks Clinical Research Associates (CRA) for permanent positions in Italy to support a global study. Ideal candidates will have a CRO background and expertise in site monitoring to ensure the timely delivery of clinical projects. Strong communication skills and a solid understanding of clinical regulations are essential for success in this role.

Competenze

• 1-4 years of experience in site monitoring within clinical research.
• Strong understanding of clinical trial regulations.
• Excellent communication and multitasking abilities.

Mansioni

• Ensure adherence to the Site Monitoring Master Plan and relevant regulations.
• Assist in identifying new potential sites for clinical trials.
• Regularly enhance technical and soft skills to improve project outcomes.

Conoscenze

Understanding of ICH GCP

Excellent verbal and written communication

Ability to multitask

Formazione

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

Descrizione del lavoro

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

We are expanding at a rapid rate and have multiple opportunities on a permanent basis to join us on a global study. Ideally you will come from a CRO background with experience across multiple therapeutic area's.

As a global contract research organization (CRO), we offer a diverse slate of clinical development and resource solutions reflecting both full-service CRO and functional service provider (FSP) models. In supporting clinical outsourcing needs for emerging biotech and pharmaceutical companies—most notably small to mid-size enterprises facing unique challenges we offer our expertise with a presence in key markets including the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia

Primary Purpose :

We are seeking skilled CRA's to ensure the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP).

Key Responsibilities :

Deliver on the Site Monitoring Plan :

Gain a comprehensive understanding of the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality 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 within various therapeutic areas to expand our clinical network. Continuous Skill Development :

Regularly enhance both technical and soft skills, applying them to elevate 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 executives.

Value Added :

Your adherence to the quality and timelines of the monitoring plan 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 Experience :

Education :

Bachelor’s or Master’s degree in a scientific discipline. Experience :

1-4 years of experience in site monitoring within clinical research. Skills :

Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask and thrive under demanding timelines.