Clinical Research Associate

JR Italy; Novara; In loco; EUR 40.000 - 80.000; Tempo pieno

Descrizione del lavoro

An established industry player is expanding its global presence and seeks skilled Clinical Research Associates (CRAs) to ensure high-quality site monitoring for clinical studies. This role offers the opportunity to work with a diverse range of therapeutic areas and contribute to the success of innovative projects. You will be pivotal in managing site compliance, identifying new potential sites, and enhancing your skills in a dynamic environment. If you possess a strong background in clinical research and are passionate about delivering quality outcomes, this position could be your next career move.

Competenze

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

Mansioni

• Ensure adherence to quality standards and timelines in site monitoring.
• Manage sites according to the Site Monitoring Master Plan.

Conoscenze

Site Monitoring

Communication Skills

ICH GCP Knowledge

Multitasking

Formazione

Bachelor’s Degree in a Scientific Discipline

Master’s Degree in a Scientific Discipline

Descrizione del lavoro

Social network you want to login/join with:

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

We are expanding rapidly and have multiple 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 offer a diverse range of clinical development and resource solutions, reflecting both 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. 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 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 standards 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 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 adherence to quality standards and timelines in monitoring activities will be vital for the successful delivery of our projects.

Key Success Factors:

• Timely and high-quality site monitoring activities.
• Prompt report generation and stakeholder communication.
• 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 and work under tight deadlines.