Clinical Research Associate

JR Italy; Reggio Emilia; In loco; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

An established industry player in clinical research is seeking skilled Clinical Research Associates (CRAs) to join their rapidly expanding team. This exciting role involves ensuring the timely and high-quality delivery of site monitoring activities for a global study. Ideal candidates will have a background in CRO with experience across various therapeutic areas. You will play a crucial role in site management compliance, site identification, and continuous skill development. Join a dynamic organization that supports clinical outsourcing needs for biotech and pharmaceutical companies, and make a significant impact on the success of clinical trials.

Competenze

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

Mansioni

• Deliver on the Site Monitoring Plan ensuring adherence to quality and timelines.
• Manage sites according to the SMMP and relevant regulations.

Conoscenze

Site Monitoring

Communication Skills

ICH GCP Understanding

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:

6891048445432299520337116

Job Views:

2

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 rapidly expanding and offer numerous permanent opportunities to join us on a global study. Ideal candidates will 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, supporting clinical outsourcing needs for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises. We have a presence in key markets including 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 and 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 various therapeutic areas to expand our clinical network.
• Continuous Skill Development: Regularly enhance technical and soft skills to improve 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 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.
• 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 clinical trial regulations; excellent communication skills; ability to multitask and work under demanding timelines.