Clinical Research Associate

JR Italy; Bergamo; In loco; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

An innovative CRO is seeking skilled Clinical Research Associates (CRAs) to join their expanding team. This role focuses on ensuring high-quality site monitoring activities for global studies. Ideal candidates will have a strong background in clinical research, excellent communication skills, and a commitment to quality. As part of a dynamic team, you will contribute to the success of projects that support emerging biotech and pharmaceutical companies. Join a forward-thinking organization that values your expertise and offers opportunities for growth and development in a collaborative environment.

Competenze

• 1-4 years of site monitoring experience in clinical research.
• Strong understanding 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.
• Identify new potential sites across various therapeutic areas.

Conoscenze

Site Monitoring

Communication Skills

ICH GCP Knowledge

Multitasking

Formazione

Bachelor’s Degree in Scientific Discipline

Master’s Degree in Scientific Discipline

Descrizione del lavoro

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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 diverse 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.

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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:

• 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 regarding 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 adherence to timelines is crucial for the successful delivery of our projects.

Key Success Factors:

• Timely and high-quality execution of site monitoring activities.
• Prompt reporting and submission of reports to stakeholders.
• Education: Bachelor’s or Master’s degree in a scientific discipline.
• Experience: 1-4 years of site monitoring experience in clinical research.
• Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication skills; ability to multitask and perform under demanding timelines.