Clinical Research Associate

JR Italy; Alessandria; In loco; EUR 35.000 - 65.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking skilled Clinical Research Associates (CRAs) to join their team for a global study. This role offers an exciting opportunity to contribute to clinical development and resource solutions. As a CRA, you will ensure the timely and high-quality delivery of site monitoring activities, adhering to the Site Monitoring Plan. With a focus on continuous skill development, you will collaborate with various stakeholders to enhance project outcomes. Join a rapidly expanding organization that values quality and efficiency in clinical research, making a meaningful impact in the biotech and pharmaceutical sectors.

Competenze

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

Mansioni

• Deliver on the Site Monitoring Plan and ensure quality adherence.
• Manage sites according to regulations to minimize QA audit observations.

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

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Client:

CliniRx

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

6891048445432299520337145

Job Views:

1

Posted:

02.05.2025

Expiry Date:

16.06.2025

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Job Description:

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

We are expanding rapidly and offer multiple permanent opportunities to join us on a global study. Candidates ideally should have a CRO background with experience across various 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, with a presence in the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.

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Primary Purpose: We seek 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 quality and adherence to timelines.
• Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize QA audit observations.
• Site Identification: Assist in identifying new potential sites across 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 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 and timelines is crucial for efficient project delivery and overall success.

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 understanding of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask and work under demanding timelines.