Research Associate

Buscojobs; Umbria; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A global clinical research organization is seeking Clinical Research Associates (CRAs) in Italy to ensure the timely delivery of site monitoring activities. Responsibilities include overseeing the Site Monitoring Plan and ensuring compliance with regulations. Candidates should possess a Bachelor's or Master's degree in a scientific discipline and 1-4 years of monitoring experience. Strong understanding of ICH GCP is essential.

Competenze

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

Mansioni

• Deliver on the Site Monitoring Plan to ensure quality and timelines.
• Manage sites according to the SMMP and relevant regulations.
• Assist in identifying new potential sites to expand clinical networks.
• Enhance technical and soft skills for performance improvement.
• Report to the Manager of Clinical Operations for project matters.
• Collaborate with the site monitoring team and administrative staff.

Conoscenze

Strong understanding of ICH GCP

Excellent verbal communication skills

Excellent written communication skills

Formazione

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

Descrizione del lavoro

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

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.

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

Responsibilities include :

• 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.
• Regularly enhance both technical and soft skills, applying them to elevate performance and project outcomes.
• 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.

Your adherence to the quality and timelines of the monitoring plan will be crucial for the efficient delivery of our projects and overall success.

Qualifications :

• 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 skills.

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